N/A Mp-0098
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841036201524 | Date22 Oct 2015 | StatusListed |
Recalls
-
- Terminated Z-1220-2017
The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Craniofacial fixation plate, non-bioabsorbable, non-customized
- Model / Reference
- MP-0098
- Primary DI / UDI-DI
- 00841036201524
- FDA Product Code
- JEY, DZJ, LLZ
- GMDN Term
- Craniofacial fixation plate, non-bioabsorbable, non-customized
- Device Class
- Class II
- Regulation Number
- 872.4760, 872.4120, 892.2050
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Biomet Microfixation, Inc
Properties
Other properties (10)
- Sterile: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No