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FDA 510(k)

PARIETENE POLYPROPYLENE MESH

K-Number: K991400 · 1999-07-12

Decision Date1999-07-12
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PARIETENE POLYPROPYLENE MESH is the device name listed in this FDA 510(k) record. The listed applicant is Sofradim Production. It received FDA 510(k) clearance on 1999-07-12 under 510(k) number K991400. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 36 devices →

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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