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FDA 510(k), K090679, VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
FDA 510(k), K090679, VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
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510(K) Number: K090679
Device Name: VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
Manufacturer: GRACE HOLLAND
Device Classification Name: Device, Anastomotic, Microvascular
Regulation Number: MVR
Classification Product Code: 03/16/2009
Date Received: 04/17/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
Manufacturer: GRACE HOLLAND
Device Classification Name: Device, Anastomotic, Microvascular
Regulation Number: MVR
Classification Product Code: 03/16/2009
Date Received: 04/17/2009
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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