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FDA 510(k)

OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR

K-Number: K990922 · 1999-06-02

ApplicantHowmedica Osteonics Corp.
Decision Date1999-06-02
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR 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 1999-06-02 under 510(k) number K990922. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR?

OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR is a medical device that received FDA 510(k) clearance on 1999-06-02. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K990922.

When did OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR receive FDA 510(k) clearance?

OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR received FDA 510(k) clearance on 1999-06-02, under 510(k) number K990922.

Who is the listed applicant for OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR?

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 OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR?

The FDA product code for OSTEONICS SPINAL SYSTEM VERSATILE CROSS CONNECTOR is KWP.

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Related Devices (Code: KWP)

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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