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FDA 510(k)

ADVANCE TIBIAL COMPONENT

K-Number: K960617 · 1996-05-08

ApplicantWrightmedicaltechnologyinc
Decision Date1996-05-08
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

ADVANCE TIBIAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1996-05-08 under 510(k) number K960617. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ADVANCE TIBIAL COMPONENT?

ADVANCE TIBIAL COMPONENT is a medical device that received FDA 510(k) clearance on 1996-05-08. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K960617.

When did ADVANCE TIBIAL COMPONENT receive FDA 510(k) clearance?

ADVANCE TIBIAL COMPONENT received FDA 510(k) clearance on 1996-05-08, under 510(k) number K960617.

Who is the listed applicant for ADVANCE TIBIAL COMPONENT?

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

What is the FDA product code for ADVANCE TIBIAL COMPONENT?

The FDA product code for ADVANCE TIBIAL COMPONENT is HRY.

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Related Devices (Code: HRY)

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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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