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FDA 510(k)

OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM

K-Number: K990712 · 1999-07-20

ApplicantHowmedica Osteonics Corp.
Decision Date1999-07-20
Product CodeMJT
DecisionSubstantially Equivalent

Device Summary

OSTEONICS SOLAR SHOULDER BIPOLAR 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 1999-07-20 under 510(k) number K990712. The device is classified under product code MJT. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM?

OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM is a medical device that received FDA 510(k) clearance on 1999-07-20. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K990712.

When did OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM receive FDA 510(k) clearance?

OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM received FDA 510(k) clearance on 1999-07-20, under 510(k) number K990712.

Who is the listed applicant for OSTEONICS SOLAR SHOULDER BIPOLAR 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 OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM?

The FDA product code for OSTEONICS SOLAR SHOULDER BIPOLAR SYSTEM is MJT.

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Related Devices (Code: MJT)

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.

K982418BUECHEL-PAPPAS MODULAR SALVAGE STEMEndotec, Inc.K960363BIPOLAR SHOULDER PROSTHESIS-SHELL(RD-113130/33, BIANGULAR MODULAR HEAD(RD-113101/41/42,BIOMODULAR MODULAR HEAD(RD-113143Biomet, Inc.

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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