Na 9510-22-800
by Zimmer, Inc. United States GUDID
Product code KXA
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024183322 | Date20 Jul 2016 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Na
- Generic Name
- Femoral head prosthesis trial
- Model / Ref / Catalog
- 9510-22-800
- Primary DI / UDI-DI
- 00889024183322
- 510(k) Number
- FDA Product Code
- KXA
- GMDN Term
- Femoral head prosthesis trial
- Device Class
- Class II
- Regulation Number
- 888.3400
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Zimmer, Inc.
Properties & raw data
Show properties, registry sources and raw records
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
Sources (1)
- FDA UDI 395a8865-9223-408d-8c0f-b7ee53420eaf