VITAMESH MACROPOROUS PP SURGICAL MESH

Mesh, Surgical, Polymeric

PROXY BIOMEDICAL LTD.

The following data is part of a premarket notification filed by Proxy Biomedical Ltd. with the FDA for Vitamesh Macroporous Pp Surgical Mesh.

Pre-market Notification Details

Device IDK060520
510k NumberK060520
Device Name:VITAMESH MACROPOROUS PP SURGICAL MESH
ClassificationMesh, Surgical, Polymeric
Applicant PROXY BIOMEDICAL LTD. P.O. BOX 560 Stillwater,  MN  55082
ContactElaine Duncan
CorrespondentElaine Duncan
PROXY BIOMEDICAL LTD. P.O. BOX 560 Stillwater,  MN  55082
Product CodeFTL  
CFR Regulation Number878.3300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2006-02-27
Decision Date2006-03-28
Summary:summary

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