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FDA 510(k), K091729, ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
FDA 510(k), K091729, ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
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510(K) Number: K091729
Device Name: ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
Manufacturer: CHRISTOPHER KLACZYK
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: LYC
Classification Product Code: 06/11/2009
Date Received: 12/23/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE
Manufacturer: CHRISTOPHER KLACZYK
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: LYC
Classification Product Code: 06/11/2009
Date Received: 12/23/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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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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