K240661
- 510(k) number
- K240661
- Device name
- Geistlich Bio-Oss®
- Applicant
- Geistlich Pharma AG CH
- Product code
- NPM — Bone Grafting Material, Animal Source
- Decision date
- 2024-07-12
- Date received
- 2024-03-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K240661.pdf
Official FDA record: K240661
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.