Na 47-2359-046-27
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 | Number00889024091412 | Date24 Sep 2015 | StatusListed |
Recalls
-
- Terminated Z-0316-2020
- Terminated Z-0311-2020
- Terminated Z-0309-2020
- Terminated Z-0310-2020
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Orthopaedic bone screw (non-sliding)
- Model / Ref / Catalog
- 47-2359-046-27
- Primary DI / UDI-DI
- 00889024091412
- FDA Product Code
- HWC, HRS
- GMDN Term
- Orthopaedic bone screw (non-sliding)
- Device Class
- Class II
- Regulation Number
- 888.3040, 888.3030
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 46 Millimeter
Other devices from Zimmer, Inc.
Properties
Other properties (8)
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No