K241674
- 510(k) number
- K241674
- Device name
- OSTEOPAL® V
- Applicant
- Heraeus Medical GmbH DE
- Product code
- LOD — Bone Cement
- Decision date
- 2024-12-05
- Date received
- 2024-06-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K241674.pdf
Official FDA record: K241674
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.