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FDA 510(k)

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM

K-Number: K020650 · 2002-03-29

ApplicantHowmedica Osteonics Corp.
Decision Date2002-03-29
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2002-03-29 under 510(k) number K020650. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM?

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K020650.

When did MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020650.

Who is the listed applicant for MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM?

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

What is the FDA product code for MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM?

The FDA product code for MODIFICATION TO REFLEX ANTERIOR CERVICAL PLATE SYSTEM is KWQ.

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Related Devices (Code: KWQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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