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FDA 510(k), K212237, 3D-Cut
FDA 510(k), K212237, 3D-Cut
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$149.00 USD
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$149.00 USD
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510(K) Number: K212237
Device Name: 3D-Cut
Manufacturer: 3D-Side SA
Device Classification Name: Orthopaedic Surgical Planning And Instrument Guides
Regulation Number: 888.3030
Classification Product Code: PBF
Date Received: 07/19/2021
Decision Date: 11/29/2021
Regulation Medical Specialty: Orthopedic
Device Name: 3D-Cut
Manufacturer: 3D-Side SA
Device Classification Name: Orthopaedic Surgical Planning And Instrument Guides
Regulation Number: 888.3030
Classification Product Code: PBF
Date Received: 07/19/2021
Decision Date: 11/29/2021
Regulation Medical Specialty: Orthopedic
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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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