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FDA 510(k)

OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS

K-Number: K990059 · 1999-01-28

ApplicantHowmedica Osteonics Corp.
Decision Date1999-01-28
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS 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 1999-01-28 under 510(k) number K990059. 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 OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS?

OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS is a medical device that received FDA 510(k) clearance on 1999-01-28. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K990059.

When did OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS receive FDA 510(k) clearance?

OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS received FDA 510(k) clearance on 1999-01-28, under 510(k) number K990059.

Who is the listed applicant for OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS?

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-EXPANDED INDICATIONS?

The FDA product code for OSTEONICS SPINAL SYSTEM-EXPANDED INDICATIONS is MNI.

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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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