510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K061892Substantially Equivalent

Propatch Soft Tissue Repair Matrix

Artivion, Inc., Kennesaw GA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K061892 is the FDA 510(k) clearance record for PROPATCH SOFT TISSUE REPAIR MATRIX, a class II device, cleared for Cryolife, Inc. on under FDA product code FTM (Mesh, Surgical). FDA records list 13 510(k) clearances for Artivion, Inc., from to . As of , FDA records show no recalls naming K061892.

Clearance record

Decision date
Received
(142 days to decision)
Product code
FTM Mesh, Surgical
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cryolife, Inc. 1655 Roberts Blvd. NW, Kennesaw GA
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