FDA 510(k), K081010, BARD 3DMAX MESH
FDA 510(k), K081010, BARD 3DMAX MESH
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$149.00 USD
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510(K) Number: K081010
Device Name: BARD 3DMAX MESH
Manufacturer: STEPHANIE BAKER
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 04/09/2008
Date Received: 10/07/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BARD 3DMAX MESH
Manufacturer: STEPHANIE BAKER
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 04/09/2008
Date Received: 10/07/2008
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery