FDA 510(k), K964970, BIOMET BONE SCREW
FDA 510(k), K964970, BIOMET BONE SCREW
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510(K) Number: K964970
Device Name: BIOMET BONE SCREW
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 12/12/1996
Decision Date: 04/03/1997
Regulation Medical Specialty: Orthopedic
Device Name: BIOMET BONE SCREW
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 12/12/1996
Decision Date: 04/03/1997
Regulation Medical Specialty: Orthopedic