FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

VitaMESH Macroporous PP Surgical Mesh

K Number: K172636 · Decision Apr 30, 2018
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
6
Review Days
241

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Basic Information

Device Name
VitaMESH Macroporous PP Surgical Mesh
K Number
K172636
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Proxy Biomedical , Ltd.
Date Received
September 1, 2017
Decision Date
April 30, 2018
Product Code
FTL
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTL Mesh, Surgical, Polymeric

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FTL), ordered by most recent decision date.

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Other Clearances by Proxy Biomedical , Ltd.

K Number Device Name
K111121 VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH
K060520 VITAMESH MACROPOROUS PP SURGICAL MESH
K052100 MODIFICATION TO MOTIFMESH SOFT TISSUE PATCH
K051245 POLYFORM SYNTHETIC MESH
K050678 MOTIFMESH SOFT TISSUE PATCH