FDA 510(k), K100152, SIRONA CAD/CAM SYSTEM
FDA 510(k), K100152, SIRONA CAD/CAM SYSTEM
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510(K) Number: K100152
Device Name: SIRONA CAD/CAM SYSTEM
Manufacturer: SIRONA DENTAL SYSTEMS GMBH
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 01/19/2010
Decision Date: 10/22/2010
Regulation Medical Specialty: Dental
Device Name: SIRONA CAD/CAM SYSTEM
Manufacturer: SIRONA DENTAL SYSTEMS GMBH
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 01/19/2010
Decision Date: 10/22/2010
Regulation Medical Specialty: Dental
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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