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FDA 510(k), K082532, STRAUMANN GUIDED INSTRUMENTS
FDA 510(k), K082532, STRAUMANN GUIDED INSTRUMENTS
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510(K) Number: K082532
Device Name: STRAUMANN GUIDED INSTRUMENTS
Manufacturer: STRAUMANN USA
Device Classification Name: Drill, Bone, Powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 09/02/2008
Decision Date: 10/21/2008
Regulation Medical Specialty: Dental
Device Name: STRAUMANN GUIDED INSTRUMENTS
Manufacturer: STRAUMANN USA
Device Classification Name: Drill, Bone, Powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 09/02/2008
Decision Date: 10/21/2008
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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