Calibrate Interbody Systems— 510(k) K243461
Substantially EquivalentAlphatec Spine, Inc.
FDA 510(k) clearance K243461 for Calibrate Interbody Systems, Substantially Equivalent on 2025-03-04. Applicant: Alphatec Spine, Inc..
Clearance details
- Applicant
- Alphatec Spine, Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carlsbad, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.