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FDA 510(k), K133884, BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
FDA 510(k), K133884, BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
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510(K) Number: K133884
Device Name: BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
Manufacturer: BIODENTA SWISS AG
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 12/20/2013
Decision Date: 06/13/2014
Regulation Medical Specialty: Dental
Device Name: BIODENTA DENTAL IMPLANT SYSTEM-BONE LEVEL TAPERED D3.0 AND L6.5MM
Manufacturer: BIODENTA SWISS AG
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 12/20/2013
Decision Date: 06/13/2014
Regulation Medical Specialty: Dental
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