SOFRADIM PARIETEX SURGICAL MESHES
K-Number: K003990 · 2001-01-24
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Device Summary
Frequently Asked Questions
What is the SOFRADIM PARIETEX SURGICAL MESHES?
SOFRADIM PARIETEX SURGICAL MESHES is a medical device that received FDA 510(k) clearance on 2001-01-24. The listed applicant is Sofradim Production. The 510(k) number is K003990.
When did SOFRADIM PARIETEX SURGICAL MESHES receive FDA 510(k) clearance?
SOFRADIM PARIETEX SURGICAL MESHES received FDA 510(k) clearance on 2001-01-24, under 510(k) number K003990.
Who is the listed applicant for SOFRADIM PARIETEX SURGICAL MESHES?
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 SOFRADIM PARIETEX SURGICAL MESHES?
The FDA product code for SOFRADIM PARIETEX SURGICAL MESHES 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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