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FDA 510(k), K132817, KIVA VCF TREATMENT SYSTEM
FDA 510(k), K132817, KIVA VCF TREATMENT SYSTEM
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510(K) Number: K132817
Device Name: KIVA VCF TREATMENT SYSTEM
Manufacturer: BENVENUE MEDICAL, INC.
Device Classification Name: cement, bone, vertebroplasty
Regulation Number: 888.3027
Classification Product Code: NDN
Date Received: 09/09/2013
Decision Date: 01/24/2014
Regulation Medical Specialty: Orthopedic
Device Name: KIVA VCF TREATMENT SYSTEM
Manufacturer: BENVENUE MEDICAL, INC.
Device Classification Name: cement, bone, vertebroplasty
Regulation Number: 888.3027
Classification Product Code: NDN
Date Received: 09/09/2013
Decision Date: 01/24/2014
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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