510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001785Substantially Equivalent

Surgisis Peripheral Vascular Patch

Cook Biotech, Inc., West Lafayette IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001785 is the FDA 510(k) clearance record for SURGISIS PERIPHERAL VASCULAR PATCH, a class II device, cleared for Cook Biotech, Inc. on under FDA product code DXZ (Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene). FDA records list 31 510(k) clearances for Cook Biotech, Inc., from to . As of , FDA records show one recall naming K001785.

Clearance record

Decision date
Received
(197 days to decision)
Product code
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene
Regulation
21 CFR 870.3470
Device class
Class II
Review panel
Cardiovascular
Applicant
Cook Biotech, Inc. 3055 Kent Ave., West Lafayette IN
510(k) summary
Summary
Third party review
No

Clearances, product code DXZ

Trailing 12 months

FDA records hold no clearances under product code DXZ in the trailing twelve months.

FDA records show no clearances under product code DXZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DXZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260