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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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