Foundation Cage
by Corelink LLC
510(k) K073440
Foundation Cage is a Class II device made by Corelink LLC, cleared under FDA 510(k) K073440 on 24 Apr 2008, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK073440 | Date24 Apr 2008 | StatusActive |
Official records
- FDA 510(k) database K073440
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MAX
- FDA applicant
- Corelink, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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