ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH
K-Number: K093932 · 2010-04-09
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Device Summary
Frequently Asked Questions
What is the ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH?
ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH is a medical device that received FDA 510(k) clearance on 2010-04-09. The listed applicant is Ethicon GmbH. The 510(k) number is K093932.
When did ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH receive FDA 510(k) clearance?
ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH received FDA 510(k) clearance on 2010-04-09, under 510(k) number K093932.
Who is the listed applicant for ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH?
The FDA 510(k) record lists Ethicon GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH?
The FDA product code for ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH 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.
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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