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FDA 510(k)

TITANIUM MESH SYSTEM

K-Number: K032371 · 2004-02-12

ApplicantEncore Medical L.P.
Decision Date2004-02-12
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM MESH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2004-02-12 under 510(k) number K032371. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM MESH SYSTEM?

TITANIUM MESH SYSTEM is a medical device that received FDA 510(k) clearance on 2004-02-12. The listed applicant is Encore Medical L.P.. The 510(k) number is K032371.

When did TITANIUM MESH SYSTEM receive FDA 510(k) clearance?

TITANIUM MESH SYSTEM received FDA 510(k) clearance on 2004-02-12, under 510(k) number K032371.

Who is the listed applicant for TITANIUM MESH SYSTEM?

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

What is the FDA product code for TITANIUM MESH SYSTEM?

The FDA product code for TITANIUM MESH SYSTEM is MQP.

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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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