FDA 510(k), K150796, Dental Bone Cutting Instruments
FDA 510(k), K150796, Dental Bone Cutting Instruments
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510(K) Number: K150796
Device Name: Dental Bone Cutting Instruments
Manufacturer: SYNTHES (USA) PRODUCTS, LLC
Device Classification Name: Driver, Wire, And Bone Drill, Manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 03/26/2015
Decision Date: 06/23/2015
Regulation Medical Specialty: Dental
Device Name: Dental Bone Cutting Instruments
Manufacturer: SYNTHES (USA) PRODUCTS, LLC
Device Classification Name: Driver, Wire, And Bone Drill, Manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 03/26/2015
Decision Date: 06/23/2015
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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