Corin Metafix Hip Stem 340.432R
by Corin Ltd
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05055196968424 | Date17 Aug 2016 | StatusListed |
Recalls
-
- Ongoing Z-1509-2022
One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.
-
- Terminated Z-2609-2021
The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Corin Metafix Hip Stem
- Generic Name
- Orthopaedic broach
- Model / Ref / Catalog
- 340.432R
- Primary DI / UDI-DI
- 05055196968424
- 510(k) Number
- FDA Product Code
- JDI, LZO
- GMDN Term
- Orthopaedic broach
- Device Class
- Class II
- Regulation Number
- 888.3350, 888.3353
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Corin Ltd
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: 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