FDA 510(k), K070015, COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT

FDA 510(k), K070015, COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT

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510(K) Number: K070015
Device Name: COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT
Manufacturer: BIOMET MANUFACTURING CORP.
Device Classification Name: bone cement
Regulation Number: 888.3027
Classification Product Code: LOD
Date Received: 01/03/2007
Decision Date: 11/30/2007
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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