`FOR THE DISTRICT OF MINNESOTA
`
`VASCULAR SOLUTIONS LLC,
`TELEFLEX INNOVATIONS S.à r.l.,
`ARROW INTERNATIONAL, INC.,
`and TELEFLEX LLC
`
`
`
`v.
`
`MEDTRONIC, INC., and
`MEDTRONIC VASCULAR, INC.,
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`Plaintiffs,
`
`Defendants.
`
`
`
`
`No. 0:19-cv-01760-PJS-TNL
`
`
`
`Jury Trial Demanded
`
`
`)
`)
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`
`PLAINTIFFS’ FIRST SUPPLEMENTAL OBJECTIONS AND RESPONSES TO
`DEFENDANTS’ INTERROGATORIES CONCERNING
`PRELMINARY INJUNCTION ISSUES
`
`Plaintiffs Vascular Solutions LLC, Teleflex Innovations S.à r.l., Arrow
`
`International, Inc., and Teleflex LLC (collectively “Plaintiffs”) hereby object and respond
`
`to Defendants Medtronic, Inc., and Medtronic Vascular, Inc.’s (“Defendant” or
`
`“Medtronic”) Interrogatories Concerning Preliminary Injunction Issues as follows:
`
`INTRODUCTION
`
`Plaintiffs will respond to Medtronic’s Interrogatories in accordance with the
`
`federal discovery rules and laws, and the rules of this Court, including but not limited to
`
`Federal Rule of Civil Procedure 26 for purposes of the preliminary injunction
`
`proceedings. Plaintiffs are only required by the Federal Rules of Civil Procedure to
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`search for and produce responsive information within their personal knowledge or from
`
`documents within their possession, custody, or control, that are located following a
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`reasonably search, including only such electronically stored information that is
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`reasonably accessible.
`
`Because this is early discovery for purposes of the preliminary injunction
`
`proceedings, a protective order has not yet been entered. Accordingly, Plaintiffs will
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`produce documents upon Defendants’ agreement that access to all documents and
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`information provided in response to these Requests and designated as
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`“CONFIDENTIAL” or “CONFIDENTIAL – ATTORNEYS’ EYES ONLY” is limited to
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`the Fredrikson and Byron law firm and Chad Hanson and Matt Anderson of Medtronic
`
`until the Court’s Protective Order is in place.
`
`Plaintiffs object to Medtronic’s “Instructions” to the extent they seek to impose
`
`obligations or requirements beyond those imposed by the Federal Rules of Civil
`
`Procedure, applicable case law, or the rules of this Court, including at least with respect
`
`to Instructions 18, 21, 23, and 24. Plaintiffs further object to Medtronic’s “Definitions”
`
`of the terms “Document,” “Date,” and “Identify” as overly broad, unduly burdensome,
`
`and not proportional to the matters at issue in limited preliminary injunction discovery.
`
`Finally, Plaintiffs object to the definition of “Teleflex,” “Plaintiffs,” “you,” and “your” as
`
`overly broad, as seeking to include entities or individuals that are not within the control
`
`of Plaintiffs and as seeking to include third parties. As used herein, “Plaintiffs” refers to
`
`the plaintiffs in this action: Vascular Solutions LLC, Teleflex Innovations S.à r.l., Arrow
`
`International, Inc., and Teleflex LLC.
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`All documents produced by Plaintiffs in response to Defendants’ Interrogatories
`
`are produced without waiver of Plaintiffs’ right to object to the production of other
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`2
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`documents. Additionally, production of a document in response to an Interrogatory is not
`
`an admission of that document’s relevance, admissibility at trial or any other objection.
`
`Plaintiffs have made every effort to provide complete answers to these
`
`Interrogatories for purposes of the preliminary injunction proceedings. However,
`
`discovery is ongoing and Plaintiffs will amend, supplement, or otherwise update their
`
`answers to these discovery requests as appropriate. Plaintiffs additionally respond to
`
`Defendants’ Interrogatories as follows:
`
`INTERROGATORIES
`
`INTERROGATORY NO. 1:
`
`Identify Teleflex’s annual sales, both in the U.S. and globally, of GuideLiner from
`2009 to the present, including the number of units sold of each available version of
`GuideLiner, the revenues received, and the average annual profit margin.
`
`RESPONSE:
`
`Pursuant to Federal Rule of Civil Procedure 33(d), Plaintiffs respond by
`
`identifying at least the documents produced as VSIQXM_E00056202, -56203, -56323, -
`
`44868, and -56294. Plaintiffs are collecting and will produce and identify additional
`
`documents from which additional information responsive to this Interrogatory can be
`
`derived or ascertained.
`
`
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`3
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`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 1, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the document produced as
`
`VSIMDT_00028305. Plaintiffs reserve the right to supplement and/or amend this
`
`Response as further relevant information is discovered during the course of this litigation.
`
`INTERROGATORY NO. 2:
`
`Identify the average annual list price and sales price of GuideLiner from 2009 to
`
`the present.
`
`RESPONSE:
`
`Pursuant to Federal Rule of Civil Procedure 33(d), Plaintiffs respond by
`
`identifying at least the document produced as VSIQXM_E00044867. Plaintiffs are
`
`collecting and will produce and identify additional documents from which additional
`
`information responsive to this Interrogatory can be derived or ascertained.
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 2, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`
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`4
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`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the documents produced as
`
`VSIMDT_00023796 and 00028305. Plaintiffs reserve the right to supplement and/or
`
`amend this Response as further relevant information is discovered during the course of
`
`this litigation.
`
`INTERROGATORY NO. 3:
`
`Identify Teleflex’s average annual market share for guide extension catheters in
`
`the U.S. from 2009 to the present.
`
`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent it calls for information not in
`
`Plaintiffs’ possession, custody, or control. Plaintiffs further object to this Interrogatory as
`
`burdensome and oppressive to the extent it seeks information that is in Defendants’
`
`possession or is available from public sources such as the internet. Plaintiffs further
`
`object to this Interrogatory to the extent it is duplicative of Medtronic’s other
`
`Interrogatories, including at least Interrogatory No. 4.
`
`Subject to and without waiving the foregoing objections, Plaintiffs respond that
`
`prior to Boston Scientific’s Guidezilla guide extension catheters entering the U.S. market
`
`in 2013, Plaintiffs believe there were no competitors to its own GuideLiner guide
`
`extension catheters in the United States. For the time period after Boston Scientific’s
`
`Guidezilla products entered the U.S. market in 2013, pursuant to Federal Rule of Civil
`
`Procedure 33(d), Plaintiffs respond by identifying at least the documents produced as
`
`VSIQXM_E00056205, -56290, -56291, and -56292. Plaintiffs are collecting and will
`
`
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`IPR2020-00131
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`produce and identify additional documents from which additional information responsive
`
`to this Interrogatory can be derived or ascertained.
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 3, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the document produced as
`
`VSIMDT_00023609. Plaintiffs reserve the right to supplement and/or amend this
`
`Response as further relevant information is discovered during the course of this litigation.
`
`INTERROGATORY NO. 4:
`
`Identify Teleflex’s average annual market share in the U.S. Interventional
`
`Cardiology Market from 2009 to the present.
`
`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent it calls for information not in
`
`Plaintiffs’ possession, custody, or control. Plaintiffs additionally object to this
`
`Interrogatory as vague and ambiguous, overly broad, unduly burdensome, and not
`
`proportional to the limited scope of the agreed preliminary injunction discovery or
`
`reasonably calculated to lead to the discovery of admissible evidence, particularly with
`
`respect to Defendants’ definition regarding the term “Interventional Cardiology Market.”
`
`In responding to this Interrogatory, Plaintiffs will interpret “U.S. Interventional
`
`
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`6
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`IPR2020-00131
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`Cardiology Market” to mean the U.S. market for guide extension catheters. Plaintiffs
`
`further object to this Interrogatory to the extent it is duplicative of Medtronic’s other
`
`Interrogatories, including at least Interrogatory No. 3.
`
`Subject to and without waiving the foregoing objections, Plaintiffs respond that
`
`prior to Boston Scientific’s Guidezilla guide extension catheter entering the U.S. market
`
`in 2013, Plaintiffs believe there were no competitors to its own GuideLiner guide
`
`extension catheters in the United States. For the time period after Boston Scientific’s
`
`Guidezilla products entered the U.S. market after 2013, pursuant to Federal Rule of Civil
`
`Procedure 33(d), Plaintiffs respond by identifying at least the documents produced as
`
`VSIQXM_E00056205, -56290, -56291, and -56292. Plaintiffs are collecting and will
`
`produce and identify additional documents from which additional information responsive
`
`to this Interrogatory can be derived or ascertained.
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 4, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the documents produced as
`
`VSIQXM_E00045369, -00045396, -00045646, -00045690, -00045792, -00056229 and
`
`VSIMDT_00023609, -00023720, -00026415, -00009268, -00009717, -00010205, -
`
`00010450, -00010751, -00010940, -00011088, -00012973. Plaintiffs reserve the right to
`
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`IPR2020-00131
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`supplement and/or amend this Response as further relevant information is discovered
`
`during the course of this litigation.
`
`INTERROGATORY NO. 5:
`
`Identify Teleflex’s competitors in the U.S. Interventional Cardiology Market,
`
`including the competitor’s name, the trade name of each identified competitor’s
`competing product(s), and, if known, the competitor’s market share for the identified
`competing products from 2009 to the present.
`
`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent it calls for information not in
`
`Plaintiffs’ possession, custody, or control. Plaintiffs further object to this Interrogatory as
`
`vague and ambiguous, overly broad, unduly burdensome, and not proportional to the
`
`limited scope of the agreed preliminary injunction discovery or reasonably calculated to
`
`lead to the discovery of admissible evidence, particularly with respect to Defendants’
`
`definition regarding the term “Interventional Cardiology Market.” In responding to this
`
`Interrogatory, Plaintiffs will interpret “U.S. Interventional Cardiology Market” to mean
`
`the U.S. market for guide extension catheters. Plaintiffs additionally object to this
`
`Interrogatory as burdensome and oppressive to the extent it seeks information that is in
`
`Defendants’ possession or is available from public sources such as the internet. Plaintiffs
`
`further object to this Interrogatory to the extent it is duplicative of Medtronic’s other
`
`Interrogatories, including at least Interrogatory No. 6.
`
`Subject to and without waiving the foregoing objections, Plaintiffs respond that
`
`their competitors in the guide extension catheter market are and have been Medtronic (all
`
`versions of the “Telescope” guide extension catheter since 2019), Boston Scientific (all
`
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`versions of the “Guidezilla” guide extension catheter since 2013), and QX Medical (all
`
`versions of the “Boosting Catheter” guide extension catheter since 2017). For the time
`
`period after Boston Scientific’s Guidezilla guide extension catheter entered the U.S.
`
`market, pursuant to Federal Rule of Civil Procedure 33(d), Plaintiffs respond by
`
`identifying at least the documents produced as VSIQXM_E00056205, -56290, -56291,
`
`and -56292. Plaintiffs are collecting and will produce and identify additional documents
`
`from which additional information responsive to this Interrogatory can be derived or
`
`ascertained.
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 5, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the documents produced as
`
`VSIQXM_E00029190, -00045329, -00045347, -00045369, -00045396, -00045646, -
`
`00045690, -00045736, -00045792, -00056229, -00056315, and VSIMDT_00023609, -
`
`00023720, -00026415, -00009717, -00010205, -00010450, -00010577, -00010751, -
`
`00010940, -00011088, -00011276, -00011448, -00011933, -00012114, -00012327, -
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`00012784, -00012973, -00013127, -00013400, -00013973, -00014204, -00014865, -
`
`00015013, -00015339, -00015825, -00016228, -00016830, -00017034, -00017390, -
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`00018215, -00018764, -00018976, -00019307, -00019553, -00019754, -00019939, -
`
`
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`9
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`IPR2020-00131
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`00020273, -00021439, -00022743, -00025905. Plaintiffs reserve the right to supplement
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`and/or amend this Response as further relevant information is discovered during the
`
`course of this litigation.
`
`INTERROGATORY NO. 6:
`
`
`Identify Teleflex’s competitors for sales of guide extension catheters, including
`the competitor’s name, the trade name of each identified competitor’s competing
`product(s), the available versions of each competing product, and, if known, the
`competitor’s U.S. market share for the identified competing products from 2009 to the
`present.
`
`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent it calls for information not in
`
`Plaintiffs’ possession, custody, or control. Plaintiffs further object to this Interrogatory as
`
`burdensome and oppressive to the extent it seeks information that is in Defendants’
`
`possession or is available from public sources such as the internet. Plaintiffs additionally
`
`object to this Interrogatory to the extent it is duplicative of Medtronic’s other
`
`Interrogatories, including at least Interrogatory No. 5.
`
`Subject to and without waiving the foregoing objections, Plaintiffs respond that
`
`their competitors in the guide extension catheter market are and have been Medtronic (all
`
`versions of the “Telescope” guide extension catheter since 2019), Boston Scientific (all
`
`versions of the “Guidezilla” guide extension catheter since 2013), and QX Medical (all
`
`versions of the “Boosting Catheter” guide extension catheter since 2017). For the time
`
`period after Boston Scientific’s Guidezilla entered the U.S. market, pursuant to Federal
`
`Rule of Civil Procedure 33(d), Plaintiffs respond by identifying at least the documents
`
`produced as VSIQXM_E00056205, -56290, -56291, and -56292. Plaintiffs are collecting
`
`
`
`10
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`Page 10
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`IPR2020-00131
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`and will produce and identify additional documents from which additional information
`
`responsive to this Interrogatory can be derived or ascertained.
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 6, and based on its continuing and reasonable investigation to date,
`
`Plaintiffs further respond to this Interrogatory as follows. Pursuant to Federal Rule of
`
`Civil Procedure 33(d), Plaintiffs respond by identifying, in addition to those documents
`
`identified in Plaintiffs’ original response, at least the documents produced as
`
`VSIQXM_E00045369, -00045396, -00045646, -00045690, -00045792, -00056229 and
`
`VSIMDT_00023609, -00023720, -00026415, -00010577, -00010639, -00010940, -
`
`00012784, -00012973, -00013127, -00013400, -00014781, -00015339, -00015825, -
`
`00016228, -00016727, -00016830, -00017034, -00017286, -00017390, -00018215, -
`
`00018764, -00018976, -00019307, -00019754, -00020273. Plaintiffs reserve the right to
`
`supplement and/or amend this Response as further relevant information is discovered
`
`during the course of this litigation.
`
`INTERROGATORY NO. 7:
`
`For each claim in the Patents-in-Suit, identify the Date of first conception and each
`
`reduction to practice, and describe the facts and circumstances relating to your contention
`of the conception and reduction to practice of the alleged invention, including, without
`limitation, where, when, how, and by whom the claim was conceived and reduced to
`practice, and identify all documents and things allegedly corroborating such conception
`and diligence in reducing the claimed invention to practice.
`
`
`
`
`11
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`IPR2020-00131
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`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent that it seeks information subject
`
`to the attorney-client privilege, work product doctrine, or any other privilege. Plaintiffs
`
`do not agree to waive any applicable privilege by its response to this Interrogatory.
`
`Plaintiffs further object to this Interrogatory as overly broad, unduly burdensome,
`
`irrelevant, and not proportional to the needs of the case at least to the extent it seeks
`
`information regarding the conception and reduction to practice for “each claim in the
`
`Patents-in-Suit,” because only a limited number of the large number of claims of the
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`Patents-in-Suit are at issue in this litigation and because not all claims asserted against
`
`Defendants in Plaintiffs’ Complaint are included in Plaintiffs’ motion for preliminary
`
`injunction.
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`Subject to and without waiving the foregoing objections, Plaintiffs respond that
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`the inventors came up with the idea for what became the GuideLiner catheter product and
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`that led to the inventions claimed in the patents-in-suit at some point in 2004 after the
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`annual Transcatheter Cardiovascular Therapeutics conference that took place in late
`
`September of that year. Pursuant to Federal Rule of Civil Procedure 33(d), Plaintiffs
`
`further respond by identifying at least the following documents: pages from Gregg
`
`Sutton’s laboratory notebook dated January 4, 2005 (VSIQXM_E00005937), Howard
`
`Root’s notes dated February 7, 2005 (VSIQXM_E00005949), and Howard Root’s market
`
`feasibility memorandum dated February 4, 2005 (VSIQXM_E00005947).
`
`FIRST SUPPLEMENTAL RESPONSE DATED SEPTEMBER 20, 2019
`
`Plaintiffs hereby incorporate its objections as if set forth verbatim. Subject to and
`
`
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`12
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`IPR2020-00131
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`without waiving the forgoing objections, in addition to the original response to
`
`Interrogatory No. 7, and based on its continuing and reasonable investigation to date,
`
`pursuant to Federal Rule of Civil Procedure 33(d), Plaintiffs further respond by
`
`identifying, in addition to those documents identified in Plaintiffs’ original response, at
`
`least the documents produced with the beginning bates number as VSIQXM_E00005944,
`
`-5952, -5955, -5987, -5988, -5990, -5991, and the documents produced with the
`
`beginning bates number as VSIMDT_00028870, -29897, -29923, -29949, -29963, -
`
`29964, -29969, -29973, -29978, -29996, -30001, -30073, -30079, -30086, -30090, -
`
`30095, -30101, -30106, -30111, -30117, -30123, -30129, -30135, -30139, -30168, -
`
`30170, -30178, -30182, -30184, -30186, -30223, -30439, -30532, -30667, -30683.
`
`Plaintiffs reserve the right to supplement and/or amend this Response as further relevant
`
`information is discovered during the course of this litigation.
`
`INTERROGATORY NO. 8:
`
`Identify each claim in the Patents-in-Suit that you have alleged or will allege is
`
`infringed by Telescope.
`
`RESPONSE:
`
`Plaintiffs object to this Interrogatory to the extent that it seeks information subject
`
`to the attorney-client privilege, work product doctrine, or any other privilege. Plaintiffs
`
`do not agree to waive any applicable privilege by its response to this Interrogatory.
`
`Plaintiffs further object to this Interrogatory as seeking information already provided in
`
`its Complaint. Plaintiffs further object to this Interrogatory as premature, particularly to
`
`the extent it requires Plaintiffs to set forth their infringement positions before the deadline
`
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`13
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`IPR2020-00131
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`for infringement contentions has been set by the court and to the extent it calls for a legal
`
`conclusion and/or expert testimony or analysis. Plaintiffs additionally object to this
`
`Interrogatory as overly broad, unduly burdensome, irrelevant, and not proportional to the
`
`needs of the case at least to the extent it seeks information regarding “each claim in the
`
`Patents-in-Suit that you have alleged or will allege is infringed by Telescope,” because
`
`not all claims asserted against Defendants in Plaintiffs’ Complaint are included in
`
`Plaintiffs’ motion for preliminary injunction.
`
` Subject to and without waiving the foregoing objections, Plaintiffs state that they
`
`have alleged that the following claims of the Patents-in-Suit are infringed by Telescope:
`
` Claims 12 and 14 of U.S. Patent No. 8,048,032
`
` Claims 12, 13, and 15 of U.S. Patent. No. RE45,380
`
` Claims 25, 36, and 37 of U.S. Patent No. RE45,776
`
` Claims 25, 33, 34, 38, and 44 of U.S. Patent No. RE47,379
`
` Claims 25, 28, 29, 32, and 48 of U.S. Patent No. RE45,760
`
`
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`IPR2020-00131
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`Dated: September 20, 2019
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`s/ J. Derek Vandenburgh
`J. Derek Vandenburgh (#224145)
`Tara C. Norgard (#307683)
`Joseph W. Winkels (#349707)
`Alexander S. Rinn (#385616)
`Shelleaha L. Jonas (#398417)
`CARLSON, CASPERS, VANDENBURGH &
`LINDQUIST, P.A.
`225 South Sixth Street, Suite 4200
`Minneapolis, Minnesota 55402
`(612) 436-9600 Telephone
`(612) 436-9605 Facsimile
`dvandenburgh@carlsoncaspers.com
`tnorgard@carlsoncaspers.com
`jwinkels@carlsoncaspers.com
`arinn@carlsoncaspers.com
`sjonas@carlsoncaspers.com
`
`Attorneys for Plaintiffs Vascular Solutions LLC,
`Teleflex Innovations S. à r.l., Arrow
`International, Inc., and Teleflex LLC
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`15
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`IPR2020-00131
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`CERTIFICATE OF SERVICE
`
`I certify that I caused to be served Plaintiffs’ First Supplemental Objections and
`
`
`
`Responses to Defendants’ Interrogatories Concerning Preliminary Injunction Issues via
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`the following email listserv, as agreed to by the parties, on the date noted below:
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`MDT-VSI@fredlaw.com
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`Dated: September 20, 2019
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`s/ J. Derek Vandenburgh
`J. Derek Vandenburgh (#224145)
`Tara C. Norgard (#307683)
`Joseph W. Winkels (#349707)
`Alexander S. Rinn (#385616)
`Shelleaha L. Jonas (#398417)
`CARLSON, CASPERS, VANDENBURGH &
`LINDQUIST, P.A.
`225 South Sixth Street, Suite 4200
`Minneapolis, Minnesota 55402
`(612) 436-9600 Telephone
`(612) 436-9605 Facsimile
`dvandenburgh@carlsoncaspers.com
`tnorgard@carlsoncaspers.com
`jwinkels@carlsoncaspers.com
`arinn@carlsoncaspers.com
`sjonas@carlsoncaspers.com
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`Page 16
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`Teleflex Ex. 2059
`Medtronic v. Teleflex
`IPR2020-00131
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