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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
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
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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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