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FDA 510(k), K140737, STRAUMANN CARES SCREW RETAINED BARS/BRIDGE
FDA 510(k), K140737, STRAUMANN CARES SCREW RETAINED BARS/BRIDGE
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510(K) Number: K140737
Device Name: STRAUMANN CARES SCREW RETAINED BARS/BRIDGE
Manufacturer: STRAUMANN USA, LLC
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 03/24/2014
Decision Date: 08/14/2014
Regulation Medical Specialty: Dental
Device Name: STRAUMANN CARES SCREW RETAINED BARS/BRIDGE
Manufacturer: STRAUMANN USA, LLC
Device Classification Name: abutment, implant, dental, endosseous
Regulation Number: 872.3630
Classification Product Code: NHA
Date Received: 03/24/2014
Decision Date: 08/14/2014
Regulation Medical Specialty: Dental
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- 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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