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FDA 510(k), K091900, ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
FDA 510(k), K091900, ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
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510(K) Number: K091900
Device Name: ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
Manufacturer: REBECCA RONNER
Device Classification Name: Staple, Implantable
Regulation Number: GDW
Classification Product Code: 06/25/2009
Date Received: 07/16/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
Manufacturer: REBECCA RONNER
Device Classification Name: Staple, Implantable
Regulation Number: GDW
Classification Product Code: 06/25/2009
Date Received: 07/16/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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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