Na 2357-07-14
by Zimmer, Inc.
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024055698 | Date28 Sep 2017 | StatusListed |
Recalls
-
- Ongoing Z-2254-2023
Thread form issue of the locking holes in that the locking screws would not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock.
-
- Terminated Z-0317-2020
- 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- Withdrawn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 fixation plate, non-bioabsorbable
- Model / Ref / Catalog
- 2357-07-14, 00-2357-007-14
- Primary DI / UDI-DI
- 00889024055698
- FDA Product Code
- HRS
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable
- Device Class
- Class II
- Regulation Number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- Size
- Length — 216 Millimeter
Other devices from Zimmer, 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