Baha 90415
by Cochlear Bone Anchored Solutions AB
Baha 90415 is a Class II device made by Cochlear Bone Anchored Solutions AB, cleared under FDA 510(k) K100360 on 13 Jul 2010 and listed in FDA GUDID since 22 Oct 2015 (UDI-DI 09321502012867), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number09321502012867 | Date22 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK100360 | Date13 Jul 2010 | StatusActive |
Official records
- AccessGUDID record 09321502012867
- FDA 510(k) database K100360
Across registries
- FDA 510(k) K100360 decided 13 Jul 2010 Active
- FDA GUDID UDI-DI 09321502012867 listed 22 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K100360
- Listed FDA GUDID 09321502012867
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Baha
- Generic name
- General external orthopaedic fixation system implantation kit, reusable
- Model / Ref / Catalog
- 90415
- Primary DI / UDI-DI
- 09321502012867
- 510(k) Number
- FDA product code
- LXB
- GMDN term
- General external orthopaedic fixation system implantation kit, reusable
- Device class
- Class II
- Regulation number
- 874.3302
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
- Size
- Length — 3 Millimeter
Similar devices in this category
Other devices filed under General external orthopaedic fixation system implantation kit, reusable.