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FDA 510(k)

MODIFICATION TO GEO STRUCTURE

K-Number: K020048 · 2002-02-06

ApplicantInterpore Cross Intl.
Decision Date2002-02-06
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO GEO STRUCTURE 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 2002-02-06 under 510(k) number K020048. 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 MODIFICATION TO GEO STRUCTURE?

MODIFICATION TO GEO STRUCTURE is a medical device that received FDA 510(k) clearance on 2002-02-06. The listed applicant is Interpore Cross Intl.. The 510(k) number is K020048.

When did MODIFICATION TO GEO STRUCTURE receive FDA 510(k) clearance?

MODIFICATION TO GEO STRUCTURE received FDA 510(k) clearance on 2002-02-06, under 510(k) number K020048.

Who is the listed applicant for MODIFICATION TO GEO STRUCTURE?

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 MODIFICATION TO GEO STRUCTURE?

The FDA product code for MODIFICATION TO GEO STRUCTURE is MQP.

Related Clinical Trials

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Other records listing Interpore Cross Intl. as applicant

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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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