Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip +7 more— 510(k) K261008

Substantially Equivalent

Stryker Spine

FDA 510(k) clearance K261008 for Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip +7 more, Substantially Equivalent on 2026-04-24. Applicant: Stryker Spine. Device class: 2.

Clearance details

Device name as filed
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 Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute
Applicant
Stryker Spine
Product code
Code MQV
Device class
Class 2
Regulation
21 CFR 888.3045
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Allendale, NJ, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code MQV

product code MQV
Death
6
Injury
435
Total
441

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.