GUIDOR BIORESORBABLE MATRIX BARRIER— 510(k) K132325
Substantially EquivalentSunstar Americas, Inc.
FDA 510(k) clearance K132325 for GUIDOR BIORESORBABLE MATRIX BARRIER, Substantially Equivalent on 2013-10-29. Applicant: Sunstar Americas, Inc.. Device class: 2.
Clearance details
- Applicant
- Sunstar Americas, Inc.
- Product code
- Code NPK
- Device class
- Class 2
- Regulation
- 21 CFR 872.3930
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- New York, NY, US
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