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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: KXA
Date Received: 03/16/2009
Decision Date: 04/17/2009
Decision: 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: KXA
Date Received: 03/16/2009
Decision Date: 04/17/2009
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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