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FDA 510(k), K133907, VSP SYSTEM
FDA 510(k), K133907, VSP SYSTEM
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510(K) Number: K133907
Device Name: VSP SYSTEM
Manufacturer: MEDICAL MODELING INC.
Device Classification Name: driver, wire, and bone drill, manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 12/23/2013
Decision Date: 01/22/2014
Regulation Medical Specialty: Dental
Device Name: VSP SYSTEM
Manufacturer: MEDICAL MODELING INC.
Device Classification Name: driver, wire, and bone drill, manual
Regulation Number: 872.4120
Classification Product Code: DZJ
Date Received: 12/23/2013
Decision Date: 01/22/2014
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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