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K242280 is the FDA 510(k) clearance record for Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, Vitoss® BiModal Bioactive Bone Graft Substitute, Vitoss BBTrauma® Bioactive Bone Graft Substitute,Vitoss® BA2X Bioactive Bone Graft Substitute, Vitoss® Bioactive Bone Graft Substitute Pack,Vitoss® Bioactive Bone Graft Substitute, Vitoss® Foam Bone Graft Substitute, Vitoss® Bone Graft Substitute Filled Canister, Vitoss® Bone Graft Substitute, Vitoss® Bone Graft Substitute - Synthetic Cancellous Chips, a class II device, cleared for Stryker Spine on under FDA product code MQV (Filler, Bone Void, Calcium Compound). FDA records list 377 510(k) clearances for HOWMEDICA OSTEONICS CORP, from to . As of , FDA records show no recalls naming K242280.
Clearance record
- Decision date
- Received
- (27 days to decision)
- Product code
- MQV Filler, Bone Void, Calcium Compound
- Regulation
- 21 CFR 888.3045
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Stryker Spine 2 Pearl Ct., Allendale NJ
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MQV
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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