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FDA 510(k), K063158, SYNTHES ANTEGRA SYSTEM
FDA 510(k), K063158, SYNTHES ANTEGRA SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K063158
Device Name: SYNTHES ANTEGRA SYSTEM
Manufacturer:
Device Classification Name: Appliance, Fixation, Spinal Intervertebral Body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 10/17/2006
Decision Date: 11/14/2006
Regulation Medical Specialty: Orthopedic
Device Name: SYNTHES ANTEGRA SYSTEM
Manufacturer:
Device Classification Name: Appliance, Fixation, Spinal Intervertebral Body
Regulation Number: 888.3060
Classification Product Code: KWQ
Date Received: 10/17/2006
Decision Date: 11/14/2006
Regulation Medical Specialty: Orthopedic
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