Anatomical Shoulder™ Fracture 01.04237.190
by Zimmer, Inc.
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024287150 | Date23 Oct 2015 | StatusListed |
Recalls
-
- Terminated Z-1895-2012
Bigliani/Flatow The Complete Shoulder Solution Trabecular Metal Glenoid Instrument Drill with Stop, 6 mm. Catalog number 47-4301-031-00 was actually packaged and labeled as catalog number 47-4307-031-00, lot 62071190.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Anatomical Shoulder™ Fracture
- Generic Name
- Joint prosthesis implantation kit, reusable
- Model / Reference
- 01.04237.190
- Primary DI / UDI-DI
- 00889024287150
- 510(k) Number
- FDA Product Code
- KWT, KWS, HSD
- GMDN Term
- Joint prosthesis implantation kit, reusable
- Device Class
- Class II
- Regulation Number
- 888.3650, 888.3660, 888.3690
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Zimmer, Inc.
Properties
Other properties (10)
- Sterile: 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