510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213125Substantially Equivalent

PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology

Synovis Life Technologies. Inc. (A Subsidiary of Baxter, St. Paul MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213125 is the FDA 510(k) clearance record for PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology, a class II device, cleared for Synovis Life Technologies. Inc. (A Subsidiary of Baxter on under FDA product code FTM (Mesh, Surgical). FDA records list one 510(k) clearance for Synovis Life Technologies. Inc. (A Subsidiary of Baxter. As of , FDA records show no recalls naming K213125.

Clearance record

Decision date
Received
(30 days to decision)
Product code
FTM Mesh, Surgical
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Synovis Life Technologies. Inc. (A Subsidiary of Baxter International Inc.), St. Paul MN
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