K233245
- 510(k) number
- K233245
- Device name
- MagnetOs Flex Matrix
- Applicant
- Kuros Biosciences B.V NL
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2023-11-21
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K233245.pdf
Official FDA record: K233245
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.