FDA 510(k), K112249, HEALIX KNOTLESS(TM) ANCHOR

FDA 510(k), K112249, HEALIX KNOTLESS(TM) ANCHOR

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510(K) Number: K112249
Device Name: HEALIX KNOTLESS(TM) ANCHOR
Manufacturer:
Device Classification Name: Fastener, Fixation, Biodegradable, Soft Tissue
Regulation Number: 888.3030
Classification Product Code: MAI
Date Received: 08/05/2011
Decision Date: 10/25/2011
Regulation Medical Specialty: Orthopedic
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