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IN.PACT AV Paclitaxel-Coated Percutaneous Transluminal Angioplasty (PTA) Balloon

FDA premarket approval P190008/S028 · decided 2024-04-23

Approval details

PMA number
P190008
Supplement
S028
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
IN.PACT AV Paclitaxel-Coated Percutaneous Transluminal Angioplasty (PTA) Balloon
Generic name
Drug-coated peripheral transluminal angioplasty catheter
Applicant
Medtronic Vascular, Inc.
Date received
2023-10-26
Decision date
2024-04-23
Days to decision
180 days
Decision code
APPR
Product code
PRC
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Rosa, CA
Statement
Approval for labeling changes to include the final study results of the IN.PACT AV Access IDE Cohort Post Approval Study

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510(k) clearances by this applicant

RecordFirmDate
Heli-FX EndoAnchor System (K182957)Medtronic Vascular, Inc.2018-11-21
Sentrant Introducer Sheath with Hydrophilic Coating (K171866)Medtronic Vascular, Inc.2017-12-20
SilverHawk Peripheral Plaque Excision System, TurboHawk Peripheral Plaque Excision System (K170191)Medtronic Vascular, Inc.2017-06-16
Heli-FX Applier, Heli-FX Guide, Ancillary EndoAnchor Cassette (K171427)Medtronic Vascular, Inc.2017-06-13
HawkOne Directional Atherectomy System (K161361)Medtronic Vascular, Inc.2016-10-14