K251885
- 510(k) number
- K251885
- Device name
- CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
- Applicant
- Providence Medical Technology, Inc. CA · US
- Product code
- MRW — System, Facet Screw Spinal Device
- Decision date
- 2025-07-10
- Date received
- 2025-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Unknown
510(k) Summary (official FDA PDF): K251885.pdf
Official FDA record: K251885
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.