VitaMESH Macroporous PP Surgical Mesh
K-Number: K172636 · 2018-04-30
ApplicantProxy Biomedical , Ltd.
Decision Date2018-04-30
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
VitaMESH Macroporous PP Surgical Mesh is a medical device manufactured by Proxy Biomedical , Ltd.. It received FDA 510(k) clearance on 2018-04-30 under approval number K172636. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VitaMESH Macroporous PP Surgical Mesh?
VitaMESH Macroporous PP Surgical Mesh is a medical device that received FDA 510(k) clearance on 2018-04-30. It is manufactured by Proxy Biomedical , Ltd.. The 510(k) number is K172636.
When was VitaMESH Macroporous PP Surgical Mesh approved by the FDA?
VitaMESH Macroporous PP Surgical Mesh received FDA 510(k) clearance on 2018-04-30, under approval number K172636.
What company makes VitaMESH Macroporous PP Surgical Mesh?
VitaMESH Macroporous PP Surgical Mesh is manufactured by Proxy Biomedical , Ltd..
What is the FDA product code for VitaMESH Macroporous PP Surgical Mesh?
The FDA product code for VitaMESH Macroporous PP Surgical Mesh is FTL.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.