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FDA 510(k)

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM

K-Number: K990959 · 1999-12-27

ApplicantSpineology, Inc.
Decision Date1999-12-27
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Spineology, Inc.. It received FDA 510(k) clearance on 1999-12-27 under 510(k) number K990959. 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 K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM?

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 1999-12-27. The listed applicant is Spineology, Inc.. The 510(k) number is K990959.

When did K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?

K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 1999-12-27, under 510(k) number K990959.

Who is the listed applicant for K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM?

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

What is the FDA product code for K-CENTRUM ANTERIOR SPINAL FIXATION SYSTEM?

The FDA product code for K-CENTRUM ANTERIOR SPINAL FIXATION 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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