FDA 510(k), K050418, TISSUE FIXATION SYSTEM
FDA 510(k), K050418, TISSUE FIXATION SYSTEM
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510(K) Number: K050418
Device Name: TISSUE FIXATION SYSTEM
Manufacturer: TFS MANUFACTURING PTY LTD
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 02/18/2005
Decision Date: 05/16/2005
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TISSUE FIXATION SYSTEM
Manufacturer: TFS MANUFACTURING PTY LTD
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 02/18/2005
Decision Date: 05/16/2005
Regulation Medical Specialty: General & Plastic Surgery