FDA 510(k)

LIAC

K-Number: K110840 · 2012-04-17

Decision Date2012-04-17

Product CodeIYE

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

LIAC is the device name listed in this FDA 510(k) record. The listed applicant is Sordina S.P.A.. It received FDA 510(k) clearance on 2012-04-17 under 510(k) number K110840. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIAC?

LIAC is a medical device that received FDA 510(k) clearance on 2012-04-17. The listed applicant is Sordina S.P.A.. The 510(k) number is K110840.

When did LIAC receive FDA 510(k) clearance?

LIAC received FDA 510(k) clearance on 2012-04-17, under 510(k) number K110840.

Who is the listed applicant for LIAC?

The FDA 510(k) record lists Sordina S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIAC?

The FDA product code for LIAC is IYE.

Related PubMed Literature

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.

PMID: 34249562Trends in Diagnosis and Treatment of Sacroiliac Joint Pathology Over the Past 10 Years: Review of Scientific Evidence for New Devices for Sacroiliac Joint Fusion.Cureus ()

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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.