RETROMTA-ORTHOMTA II— 510(k) K132825
Substantially EquivalentBiomta
FDA 510(k) clearance K132825 for RETROMTA-ORTHOMTA II, Substantially Equivalent on 2014-04-10. Applicant: Biomta. Device class: 2.
Clearance details
- Applicant
- Biomta
- Product code
- Code KIF
- Device class
- Class 2
- Regulation
- 21 CFR 872.3820
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fullerton, CA, US
Recent devices under product code KIF
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