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FDA 510(k)

XIA SPINAL SYSTEM

K-Number: K022160 · 2002-08-01

ApplicantHowmedica Osteonics
Decision Date2002-08-01
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

XIA SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K022160. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XIA SPINAL SYSTEM?

XIA SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Howmedica Osteonics. The 510(k) number is K022160.

When did XIA SPINAL SYSTEM receive FDA 510(k) clearance?

XIA SPINAL SYSTEM received FDA 510(k) clearance on 2002-08-01, under 510(k) number K022160.

Who is the listed applicant for XIA SPINAL SYSTEM?

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

What is the FDA product code for XIA SPINAL SYSTEM?

The FDA product code for XIA SPINAL SYSTEM is MNI.

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Other records listing Howmedica Osteonics as applicant

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Related Devices (Code: MNI)

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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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