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PORCINE SURGICAL MESH - Porcine Surgical Mesh

by Brennen Medical, LLC

510(k) K081272

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

4 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK081272 Date31 Jul 2008ClearedStatusActive

Recalls

4 recalls · FDA

  • 4 recalls, same reason

    • Terminated Z-1379-2011 FDA Unclassified (pre-2012) initiated 7 Jan 2011
    • Terminated Z-1381-2011 FDA Unclassified (pre-2012) initiated 7 Jan 2011
    • Terminated Z-1380-2011 FDA Unclassified (pre-2012) initiated 7 Jan 2011
    • Terminated Z-1382-2011 FDA Unclassified (pre-2012) initiated 7 Jan 2011

    Davol cannot guarantee that all Xenomatic product released from July to October 2010 meets FDA guidelines for endotoxin limits; and therefore, the grafts are potentially contaminated with bacteria.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
FTM
Models / Variants
Porcine Surgical Mesh
Device Class
Class II
Regulation
21 CFR Part 878.3300
Advisory Committee
General, Plastic Surgery
FDA Decision
SESE Substantially Equivalent

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