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FDA 510(k), K071726, ZUMA
FDA 510(k), K071726, ZUMA
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510(K) Number: K071726
Device Name: ZUMA
Manufacturer: ETHEL BERNAL
Device Classification Name: Spinal Vertebral Body Replacement Device
Regulation Number: MQP
Classification Product Code: 06/25/2007
Date Received: 10/23/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: ZUMA
Manufacturer: ETHEL BERNAL
Device Classification Name: Spinal Vertebral Body Replacement Device
Regulation Number: MQP
Classification Product Code: 06/25/2007
Date Received: 10/23/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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