FDA 510(k), K091207, SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE

FDA 510(k), K091207, SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE

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510(K) Number: K091207
Device Name: SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE
Manufacturer:
Device Classification Name: Washer, Bolt Nut
Regulation Number: 888.3030
Classification Product Code: HTN
Date Received: 04/24/2009
Decision Date: 02/15/2011
Regulation Medical Specialty: Orthopedic
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