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COMPLETE SE VASCULAR STENT SYSTEM-SFA AND PPA

FDA premarket approval P110040/S011 · decided 2017-02-01

Approval details

PMA number
P110040
Supplement
S011
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
COMPLETE SE VASCULAR STENT SYSTEM-SFA AND PPA
Generic name
STENT, SUPERFICIAL FEMORAL ARTERY
Applicant
Medtronic Vascular
Date received
2016-08-17
Decision date
2017-02-01
Days to decision
168 days
Decision code
APPR
Product code
NIP
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Rosa, CA
Statement
Approval for updated in-process sampling requirements and to remove redundant inspections.

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510(k) clearances by this applicant

RecordFirmDate
Steerantâ„¢ Super Stiff Guidewire (K232570)Medtronic Vascular2023-10-24
6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter (K232190)Medtronic Vascular2023-08-22
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Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P) (K220773)Medtronic Vascular2022-04-13
Medtronic 6F Taiga Guiding Catheter (K192296)Medtronic Vascular2019-09-20
Admiral Xtreme (K173515)Medtronic Vascular2018-04-12
InTRAkit (K162097)Medtronic Vascular2016-11-17
TRAcelet Compression Device (K162027)Medtronic Vascular2016-10-21