FDA 510(k), K070173, VERTE-STACK SPINAL SYSTEM

FDA 510(k), K070173, VERTE-STACK SPINAL SYSTEM

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510(K) Number: K070173
Device Name: VERTE-STACK SPINAL SYSTEM
Manufacturer:
Device Classification Name: Spinal Vertebral Body Replacement Device
Regulation Number: 888.3060
Classification Product Code: MQP
Date Received: 01/18/2007
Decision Date: 03/14/2007
Regulation Medical Specialty: Orthopedic
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