SwissGraft X— 510(k) K251613
Substantially EquivalentGeistlich Pharma AG
FDA 510(k) clearance K251613 for SwissGraft X, Substantially Equivalent on 2025-06-26. Applicant: Geistlich Pharma AG. Device class: 2.
Clearance details
- Applicant
- Geistlich Pharma AG
- Product code
- Code NPM
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Wolhusen, CH
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