Ac Device LD090
Ac Device LD090 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 05060433600043), 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 | Number05060433600043 | Date30 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK091207 | Date15 Feb 2011 | StatusActive |
Official records
- AccessGUDID record 05060433600043
- FDA 510(k) database K091207
Across registries
- FDA 510(k) K091207 decided 15 Feb 2011 Active
- FDA GUDID UDI-DI 05060433600043 listed 30 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K091207
- Listed FDA GUDID 05060433600043
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- Withdrawn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
- LD090
- Primary DI / UDI-DI
- 05060433600043
- 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 — 9 Centimeter
Similar devices
Other devices filed under FDA product code HTN (Washer, Bolt Nut).
- BONE-LOK HP WASHER by Triage Medical, Inc.
- NON-LOCKING SCREW 1312-20-515 131220515 by Biomet Orthopedics, Inc.
- A.L.P.S.® 8563-27-038 856327038 by Biomet Orthopedics, Inc.
- M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System 03.65.705 by Medacta International SA
- MINI TIGHTROPE by Arthrex, Inc.
- HEX BUTTON by Pioneer Surgical Technology, Inc.
- 390017 by Stryker GmbH
- RONDO' VP-91130 by Citieffe
- TriMed Ripcord Device by Trimed, INC.
- 4845-50-01 00-4845-050-01 by Zimmer, Inc.