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FDA 510(k)

TITANIUM MESH IMPLANT

K-Number: K041407 · 2004-12-29

ApplicantInterpore Cross Intl.
Decision Date2004-12-29
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM MESH IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Cross Intl.. It received FDA 510(k) clearance on 2004-12-29 under 510(k) number K041407. 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 IMPLANT?

TITANIUM MESH IMPLANT is a medical device that received FDA 510(k) clearance on 2004-12-29. The listed applicant is Interpore Cross Intl.. The 510(k) number is K041407.

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

TITANIUM MESH IMPLANT received FDA 510(k) clearance on 2004-12-29, under 510(k) number K041407.

Who is the listed applicant for TITANIUM MESH IMPLANT?

The FDA 510(k) record lists Interpore Cross Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM MESH IMPLANT?

The FDA product code for TITANIUM MESH IMPLANT is MQP.

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Other records listing Interpore Cross Intl. 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.

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Related Devices (Code: 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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