PORCINE SURGICAL MESH - Porcine Surgical Mesh
510(k) K081272
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK081272 | Date31 Jul 2008 | StatusActive |
Recalls
-
- Terminated Z-1379-2011
- Terminated Z-1381-2011
- Terminated Z-1380-2011
- Terminated Z-1382-2011
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
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 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