K260364
- 510(k) number
- K260364
- Device name
- Device 300419 Strip
- Applicant
- Geistlich Pharma AG CH
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2026-06-02
- Date received
- 2026-02-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K260364.pdf
Official FDA record: K260364
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.