N/A 4921-2-020
by Stryker Sustainability Solutions United States GUDID
Product code KTT
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00885825020835 | Date23 Sep 2016 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- N/A
- Generic Name
- External orthopaedic fixation system reprocessed component
- Model / Ref / Catalog
- N/A, 4921-2-020
- Primary DI / UDI-DI
- 00885825020835
- 510(k) Number
- FDA Product Code
- KTT
- GMDN Term
- External orthopaedic fixation system reprocessed component
- Device Class
- Class II
- Regulation Number
- 888.3030
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- MRI Safety
- MR Safe
Other devices from Stryker Sustainability Solutions
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- 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
- Manufacturing Date: No
Sources (1)
- FDA UDI ae9c29ee-1c95-4938-8c38-55df8174588c