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FDA 510(k)

MICHELSON ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K974435 · 1998-02-19

ApplicantWrightmedicaltechnologyinc
Decision Date1998-02-19
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

MICHELSON ANTERIOR CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 1998-02-19 under 510(k) number K974435. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MICHELSON ANTERIOR CERVICAL PLATE SYSTEM?

MICHELSON ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1998-02-19. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K974435.

When did MICHELSON ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

MICHELSON ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 1998-02-19, under 510(k) number K974435.

Who is the listed applicant for MICHELSON ANTERIOR CERVICAL PLATE SYSTEM?

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 MICHELSON ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for MICHELSON ANTERIOR CERVICAL PLATE SYSTEM is KWQ.

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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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