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FDA 510(k)

ATRIUM CENTRILFX MESH

K-Number: K110110 · 2011-02-15

ApplicantAtrium Medical Corporation
Decision Date2011-02-15
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ATRIUM CENTRILFX MESH is the device name listed in this FDA 510(k) record. The listed applicant is Atrium Medical Corporation. It received FDA 510(k) clearance on 2011-02-15 under 510(k) number K110110. 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 ATRIUM CENTRILFX MESH?

ATRIUM CENTRILFX MESH is a medical device that received FDA 510(k) clearance on 2011-02-15. The listed applicant is Atrium Medical Corporation. The 510(k) number is K110110.

When did ATRIUM CENTRILFX MESH receive FDA 510(k) clearance?

ATRIUM CENTRILFX MESH received FDA 510(k) clearance on 2011-02-15, under 510(k) number K110110.

Who is the listed applicant for ATRIUM CENTRILFX MESH?

The FDA 510(k) record lists Atrium Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATRIUM CENTRILFX MESH?

The FDA product code for ATRIUM CENTRILFX MESH is FTL.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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