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FDA 510(k)

MODIFICATION TO CENTAUR SPINAL SYSTEM

K-Number: K001844 · 2000-07-19

ApplicantHowmedica Osteonics Corp.
Decision Date2000-07-19
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO CENTAUR SPINAL 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 2000-07-19 under 510(k) number K001844. 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 CENTAUR SPINAL SYSTEM?

MODIFICATION TO CENTAUR SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2000-07-19. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K001844.

When did MODIFICATION TO CENTAUR SPINAL SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO CENTAUR SPINAL SYSTEM received FDA 510(k) clearance on 2000-07-19, under 510(k) number K001844.

Who is the listed applicant for MODIFICATION TO CENTAUR SPINAL 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 CENTAUR SPINAL SYSTEM?

The FDA product code for MODIFICATION TO CENTAUR SPINAL SYSTEM is KWQ.

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Related Devices (Code: 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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