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FDA 510(k), K052607, ARTHREX INTERFERENCE SCREW-ROUNDED HEAD SCREWS, FULL THREADED SCREWS, SHEATHED CANNULATED INTERFERENCE SCREWS
FDA 510(k), K052607, ARTHREX INTERFERENCE SCREW-ROUNDED HEAD SCREWS, FULL THREADED SCREWS, SHEATHED CANNULATED INTERFERENCE SCREWS
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510(K) Number: K052607
Device Name: ARTHREX INTERFERENCE SCREW-ROUNDED HEAD SCREWS, FULL THREADED SCREWS, SHEATHED CANNULATED INTERFERENCE SCREWS
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 09/22/2005
Decision Date: 11/07/2005
Regulation Medical Specialty: Orthopedic
Device Name: ARTHREX INTERFERENCE SCREW-ROUNDED HEAD SCREWS, FULL THREADED SCREWS, SHEATHED CANNULATED INTERFERENCE SCREWS
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 09/22/2005
Decision Date: 11/07/2005
Regulation Medical Specialty: Orthopedic
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