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FDA 510(k)

ADVANCE SPIKED POROUS TIBIAL BASE

K-Number: K063128 · 2007-03-21

ApplicantWrightmedicaltechnologyinc
Decision Date2007-03-21
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADVANCE SPIKED POROUS TIBIAL BASE is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2007-03-21 under 510(k) number K063128. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE SPIKED POROUS TIBIAL BASE?

ADVANCE SPIKED POROUS TIBIAL BASE is a medical device that received FDA 510(k) clearance on 2007-03-21. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K063128.

When did ADVANCE SPIKED POROUS TIBIAL BASE receive FDA 510(k) clearance?

ADVANCE SPIKED POROUS TIBIAL BASE received FDA 510(k) clearance on 2007-03-21, under 510(k) number K063128.

Who is the listed applicant for ADVANCE SPIKED POROUS TIBIAL BASE?

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 SPIKED POROUS TIBIAL BASE?

The FDA product code for ADVANCE SPIKED POROUS TIBIAL BASE is MBH.

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Related Devices (Code: MBH)

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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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