K252085
- 510(k) number
- K252085
- Device name
- Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)
- Applicant
- Wright Medical Technology, Inc. (Stryker Corporation) TN · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2025-09-30
- Date received
- 2025-07-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252085.pdf
Official FDA record: K252085
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.