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FDA 510(k), K021932, SYNTHES 6.5 MM CANNULATED SCREW
FDA 510(k), K021932, SYNTHES 6.5 MM CANNULATED SCREW
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510(K) Number: K021932
Device Name: SYNTHES 6.5 MM CANNULATED SCREW
Manufacturer: SYNTHES (USA)
Device Classification Name: screw, fixation, bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 06/12/2002
Decision Date: 09/06/2002
Regulation Medical Specialty: Orthopedic
Device Name: SYNTHES 6.5 MM CANNULATED SCREW
Manufacturer: SYNTHES (USA)
Device Classification Name: screw, fixation, bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 06/12/2002
Decision Date: 09/06/2002
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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