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FDA 510(k), K024060, MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM
FDA 510(k), K024060, MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K024060
Device Name: MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 12/09/2002
Decision Date: 12/20/2002
Regulation Medical Specialty: Orthopedic
Device Name: MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 12/09/2002
Decision Date: 12/20/2002
Regulation Medical Specialty: Orthopedic
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