Taylor Spatial Frame 71070286
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20885556119376 | Date29 Aug 2015 | StatusListed |
Recalls
-
- Ongoing Z-0245-2022
Medicalplastic s.r.l. is conducting a voluntary field action to remove a group of Ilizarov Wire Tensioners due to a manufacturing error. An internal washer of the Ilizarov Wire Tensioner has been made in a wrong plastic material that could wear and break during the sterilization process in autoclave. Consequently this could cause malfunctioning of the tensioner.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Taylor Spatial Frame
- Generic Name
- External orthopaedic fixation system, single-use
- Model / Ref / Catalog
- 71070286
- Primary DI / UDI-DI
- 20885556119376
- 510(k) Number
- FDA Product Code
- KTT
- GMDN Term
- External orthopaedic fixation system, single-use
- Device Class
- Class II
- Regulation Number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
- MRI Safety
- MR Conditional
Other devices from Smith & Nephew, 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