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FDA 510(k), K923869, CODMAN SOF'WIRE TITANIUM CABLE SYSTEM
FDA 510(k), K923869, CODMAN SOF'WIRE TITANIUM CABLE SYSTEM
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510(K) Number: K923869
Device Name: CODMAN SOF'WIRE TITANIUM CABLE SYSTEM
Manufacturer: Codman & Shurtleff, Inc.
Device Classification Name: cerclage, fixation
Regulation Number: 888.3010
Classification Product Code: JDQ
Date Received: 08/03/1992
Decision Date: 05/12/1993
Regulation Medical Specialty: Orthopedic
Device Name: CODMAN SOF'WIRE TITANIUM CABLE SYSTEM
Manufacturer: Codman & Shurtleff, Inc.
Device Classification Name: cerclage, fixation
Regulation Number: 888.3010
Classification Product Code: JDQ
Date Received: 08/03/1992
Decision Date: 05/12/1993
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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