CAPRI Corpectomy Cage System
by K2M, Inc.
510(k) K211320
CAPRI Corpectomy Cage System is a Class II device made by K2M, Inc., cleared under FDA 510(k) K211320 on 24 Feb 2022, 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 | NumberK211320 | Date24 Feb 2022 | StatusActive |
Official records
- FDA 510(k) database K211320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- PLR
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3060
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Similar devices
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- ALTA Anterior Cervical Corpectomy System by Astura Medical
- Bengal Stackable Cage System by MEDOS INTERNATIONAL SARL
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- Galileo Vertebral Body Replacement Device by Bright Spine
- MediExpand Cervical Expandable VBR System by Cmf Medicon Surgical, Inc.
- VLIFT-s Vertebral Body Replacement System by Stryker Spine