K242510
- 510(k) number
- K242510
- Device name
- Geistlich Bio-Flow®
- Applicant
- Geistlich Pharma AG CH
- Product code
- NPM — Bone Grafting Material, Animal Source
- Decision date
- 2025-03-07
- Date received
- 2024-08-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K242510.pdf
Official FDA record: K242510
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.