MOTIFMESH SOFT TISSUE PATCH
K-Number: K050678 · 2005-05-20
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Device Summary
Frequently Asked Questions
What is the MOTIFMESH SOFT TISSUE PATCH?
MOTIFMESH SOFT TISSUE PATCH is a medical device that received FDA 510(k) clearance on 2005-05-20. The listed applicant is Proxy Biomedical , Ltd.. The 510(k) number is K050678.
When did MOTIFMESH SOFT TISSUE PATCH receive FDA 510(k) clearance?
MOTIFMESH SOFT TISSUE PATCH received FDA 510(k) clearance on 2005-05-20, under 510(k) number K050678.
Who is the listed applicant for MOTIFMESH SOFT TISSUE PATCH?
The FDA 510(k) record lists Proxy Biomedical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOTIFMESH SOFT TISSUE PATCH?
The FDA product code for MOTIFMESH SOFT TISSUE PATCH is FTL.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Proxy Biomedical , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FTL)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.
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