510(k) K242280
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Stryker Spine
— Product Code MQV
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 29, 2024
- Date Received
- August 2, 2024
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Filler, Bone Void, Calcium Compound
- Device Class
- Class II
- Regulation Number
- 888.3045
- Review Panel
- OR
- Submission Type