PARIETEX MONOFILAMENT POLYESTER MESH
K-Number: K090858 · 2009-05-06
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Device Summary
Frequently Asked Questions
What is the PARIETEX MONOFILAMENT POLYESTER MESH?
PARIETEX MONOFILAMENT POLYESTER MESH is a medical device that received FDA 510(k) clearance on 2009-05-06. The listed applicant is Sofradim Production. The 510(k) number is K090858.
When did PARIETEX MONOFILAMENT POLYESTER MESH receive FDA 510(k) clearance?
PARIETEX MONOFILAMENT POLYESTER MESH received FDA 510(k) clearance on 2009-05-06, under 510(k) number K090858.
Who is the listed applicant for PARIETEX MONOFILAMENT POLYESTER 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 MONOFILAMENT POLYESTER MESH?
The FDA product code for PARIETEX MONOFILAMENT POLYESTER 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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