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FDA 510(k), K895766, ASNIS II GUIDED BONE SCREW
FDA 510(k), K895766, ASNIS II GUIDED BONE SCREW
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$149.00 USD
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$149.00 USD
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510(K) Number: K895766
Device Name: ASNIS II GUIDED BONE SCREW
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 09/26/1989
Decision Date: 11/08/1989
Regulation Medical Specialty: Orthopedic
Device Name: ASNIS II GUIDED BONE SCREW
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 09/26/1989
Decision Date: 11/08/1989
Regulation Medical Specialty: Orthopedic
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