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FDA 510(k), K203712, The Slide
FDA 510(k), K203712, The Slide
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510(K) Number: K203712
Device Name: The Slide
Manufacturer: Biotex, Inc.
Device Classification Name: Device, Jaw Repositioning
Regulation Number: 872.5570
Classification Product Code: LQZ
Date Received: 12/21/2020
Decision Date: 07/20/2021
Regulation Medical Specialty: Dental
Device Name: The Slide
Manufacturer: Biotex, Inc.
Device Classification Name: Device, Jaw Repositioning
Regulation Number: 872.5570
Classification Product Code: LQZ
Date Received: 12/21/2020
Decision Date: 07/20/2021
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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