Perfuse 800-0541
Perfuse 800-0541 is a Class II device made by Biomet Biologics, LLC, cleared under FDA 510(k) K141762 on 27 Aug 2014 and listed in FDA GUDID since 3 Nov 2016 (UDI-DI 00880304999602), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00880304999602 | Date3 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK141762 | Date27 Aug 2014 | StatusActive |
Official records
- AccessGUDID record 00880304999602
- FDA 510(k) database K141762
Across registries
- FDA 510(k) K141762 decided 27 Aug 2014 Active
- FDA GUDID UDI-DI 00880304999602 listed 3 Nov 2016 Listed
Recalls
-
- Terminated Z-1814-2016
The Trocar and Plunger Assemblies are missing from the instrument, which could result in a delay in surgery greater than 30 minutes.
Timeline
- Cleared FDA 510(k) K141762
- Recall initiated FDA recalls Z-1814-2016
- Listed FDA GUDID 00880304999602
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Perfuse
- Generic name
- Bone trephine, reusable
- Model / Ref / Catalog
- 800-0541
- Primary DI / UDI-DI
- 00880304999602
- 510(k) Number
- FDA product code
- FMF
- GMDN term
- Bone trephine, reusable
- Device class
- Class II
- Regulation number
- 880.5860
- GUDID distribution status
- In Commercial Distribution
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