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
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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