FDA 510(k), K093932, ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH

FDA 510(k), K093932, ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH

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510(K) Number: K093932
Device Name: ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH
Manufacturer: NEELU MEDHEKAR
Device Classification Name: Mesh, Surgical, Polymeric
Regulation Number: FTL
Classification Product Code: 12/22/2009
Date Received: 04/09/2010
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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