Tack Endovascular System (4F, 1.5-4.5mm)

FDA Premarket Approval P190027

Pre-market Approval Supplement Details

Approval for use in mid/distal popliteal, tibial and peroneal arteries, ranging in diameter from 1. 5 mm to 4. 5 mm, for the repair of post percutaneous transluminal balloon angioplasty (pta) dissection(s).

DeviceTack Endovascular System (4F, 1.5-4.5mm)
Generic NameScaffold, Dissection Repair
ApplicantIntact Vascular, Inc.
Date Received2019-10-01
Decision Date2020-04-10
PMAP190027
SupplementS
Product CodeQCT 
Advisory CommitteeCardiovascular
Expedited ReviewNo
Combination Product No
Applicant Address Intact Vascular, Inc. 1285 Drummers Lane, #200 wayne, PA 19087

Supplemental Filings

Supplement NumberDateSupplement Type
P190027Original Filing
S005 2022-08-29 Normal 180 Day Track No User Fee
S004 2022-02-23 Normal 180 Day Track
S003
S002 2021-09-08 30-day Notice
S001 2020-09-01 30-day Notice

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.