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FDA 510(k), K171958, PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE
FDA 510(k), K171958, PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE
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510(K) Number: K171958
Device Name: PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE
Manufacturer: Mectron SPA
Device Classification Name: drill, bone, powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 06/29/2017
Decision Date: 01/12/2018
Regulation Medical Specialty: Dental
Device Name: PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE
Manufacturer: Mectron SPA
Device Classification Name: drill, bone, powered
Regulation Number: 872.4120
Classification Product Code: DZI
Date Received: 06/29/2017
Decision Date: 01/12/2018
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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