OSTEOPAL® V
FDA 510(k) clearance K241674 · decided 2024-12-05
Clearance details
- K-number
- K241674
- Device name
- OSTEOPAL® V
- Applicant
- Heraeus Medical GmbH
- Decision
- Substantially Equivalent
- Date received
- 2024-06-11
- Decision date
- 2024-12-05
- Days to decision
- 177 days
- Clearance type
- Traditional
- Product code
- LOD
- Device class
- 2
- Regulation number
- 888.3027
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Wehrheim, DE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.