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FDA 510(k), K151295, Biodenta Customized Abutment - Titanium
FDA 510(k), K151295, Biodenta Customized Abutment - Titanium
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510(K) Number: K151295
Device Name: Biodenta Customized Abutment - Titanium
Manufacturer: BIODENTA SWISS AG
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 05/15/2015
Decision Date: 12/01/2015
Regulation Medical Specialty: Dental
Device Name: Biodenta Customized Abutment - Titanium
Manufacturer: BIODENTA SWISS AG
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 05/15/2015
Decision Date: 12/01/2015
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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