Jason membrane— 510(k) K242817
Substantially EquivalentBotiss Biomaterials GmbH
FDA 510(k) clearance K242817 for Jason membrane, Substantially Equivalent on 2025-12-12. Applicant: Botiss Biomaterials GmbH. Device class: 2.
Clearance details
- Applicant
- Botiss Biomaterials GmbH
- Product code
- Code NPL
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Zossen, DE
Recent devices under product code NPL
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