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FDA 510(k)

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)

K-Number: K022143 · 2003-01-23

ApplicantInterpore Cross Intl.
Decision Date2003-01-23
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD) 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 2003-01-23 under 510(k) number K022143. 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 INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)?

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD) is a medical device that received FDA 510(k) clearance on 2003-01-23. The listed applicant is Interpore Cross Intl.. The 510(k) number is K022143.

When did INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD) receive FDA 510(k) clearance?

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD) received FDA 510(k) clearance on 2003-01-23, under 510(k) number K022143.

Who is the listed applicant for INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)?

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 INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)?

The FDA product code for INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD) 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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