PARIETENE POLYPROPYLENE MESH
K-Number: K991400 · 1999-07-12
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Device Summary
Frequently Asked Questions
What is the PARIETENE POLYPROPYLENE MESH?
PARIETENE POLYPROPYLENE MESH is a medical device that received FDA 510(k) clearance on 1999-07-12. The listed applicant is Sofradim Production. The 510(k) number is K991400.
When did PARIETENE POLYPROPYLENE MESH receive FDA 510(k) clearance?
PARIETENE POLYPROPYLENE MESH received FDA 510(k) clearance on 1999-07-12, under 510(k) number K991400.
Who is the listed applicant for PARIETENE POLYPROPYLENE 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 PARIETENE POLYPROPYLENE MESH?
The FDA product code for PARIETENE POLYPROPYLENE 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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