PARIETEX OPTIMIZED COMPOSTIE MESH
K-Number: K110815 · 2011-04-19
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Device Summary
Frequently Asked Questions
What is the PARIETEX OPTIMIZED COMPOSTIE MESH?
PARIETEX OPTIMIZED COMPOSTIE MESH is a medical device that received FDA 510(k) clearance on 2011-04-19. The listed applicant is Sofradim Production. The 510(k) number is K110815.
When did PARIETEX OPTIMIZED COMPOSTIE MESH receive FDA 510(k) clearance?
PARIETEX OPTIMIZED COMPOSTIE MESH received FDA 510(k) clearance on 2011-04-19, under 510(k) number K110815.
Who is the listed applicant for PARIETEX OPTIMIZED COMPOSTIE MESH?
The FDA 510(k) record lists Sofradim Production as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARIETEX OPTIMIZED COMPOSTIE MESH?
The FDA product code for PARIETEX OPTIMIZED COMPOSTIE 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.
Other records listing Sofradim Production 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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