InterCollagen® Guide— 510(k) K223912
Substantially EquivalentSigmagraft, Inc.
FDA 510(k) clearance K223912 for InterCollagen® Guide, Substantially Equivalent on 2023-08-17. Applicant: Sigmagraft, Inc.. Device class: 2.
Clearance details
- Applicant
- Sigmagraft, Inc.
- 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
- Fullerton, CA, US
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