510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062729Substantially Equivalent

Surgisis Rvp Recto-Vaginal Fistula Plug

Cook Biotech, Inc., Lafeyette IN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062729 is the FDA 510(k) clearance record for SURGISIS RVP RECTO-VAGINAL FISTULA PLUG, a class II device, cleared for Cook Biotech, Inc. on under FDA product code FTM (Mesh, Surgical). FDA records list 31 510(k) clearances for Cook Biotech, Inc., from to . As of , FDA records show 12 recalls naming K062729.

Clearance record

Decision date
Received
(27 days to decision)
Product code
FTM Mesh, Surgical
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cook Biotech, Inc. 1400 Cumberland Ave., Lafeyette IN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTM

Trailing 12 months
1 clearance under product code FTM in the twelve months to October 2026, August 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260