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FDA 510(k), K090083, CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
FDA 510(k), K090083, CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
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510(K) Number: K090083
Device Name: CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
Manufacturer: STAN YANG
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: LYC
Classification Product Code: 01/12/2009
Date Received: 03/23/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: CYTOFLEX RESORB, MODEL C03-0010 THROUGH C03-090
Manufacturer: STAN YANG
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: LYC
Classification Product Code: 01/12/2009
Date Received: 03/23/2009
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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