Ac Device LD080
Ac Device LD080 is a Class II device made by Lockdown Medical Ltd, cleared under FDA 510(k) K091207 on 15 Feb 2011 and listed in FDA GUDID since 30 Oct 2015 (UDI-DI 05060433600036), 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 | Number05060433600036 | Date30 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK091207 | Date15 Feb 2011 | StatusActive |
Official records
- AccessGUDID record 05060433600036
- FDA 510(k) database K091207
Across registries
- FDA 510(k) K091207 decided 15 Feb 2011 Active
- FDA GUDID UDI-DI 05060433600036 listed 30 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K091207
- Listed FDA GUDID 05060433600036
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Ac Device
- Generic name
- Ligament graft, synthetic polymer
- Model / Ref / Catalog
- LD080
- Primary DI / UDI-DI
- 05060433600036
- 510(k) Number
- FDA product code
- HTN
- GMDN term
- Ligament graft, synthetic polymer
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 8 Centimeter
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