FDA 510(k) Applications Submitted by PROXY BIOMEDICAL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K172636 09/01/2017 VitaMESH Macroporous PP Surgical Mesh Proxy Biomedical Ltd.
K060520 02/27/2006 VITAMESH MACROPOROUS PP SURGICAL MESH PROXY BIOMEDICAL LTD.
K050678 03/16/2005 MOTIFMESH SOFT TISSUE PATCH PROXY BIOMEDICAL LTD.
K111121 04/21/2011 VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH PROXY BIOMEDICAL LTD.
K051245 05/16/2005 POLYFORM SYNTHETIC MESH PROXY BIOMEDICAL LTD.
K052100 08/03/2005 MODIFICATION TO MOTIFMESH SOFT TISSUE PATCH PROXY BIOMEDICAL LTD.


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