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FDA 510(k)

STELLITE COBALT/CHROMIUM BASE METAL ALLOY

K-Number: K900117 · 1990-04-02

Decision Date1990-04-02
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STELLITE COBALT/CHROMIUM BASE METAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is D.C. Dental Specialties. It received FDA 510(k) clearance on 1990-04-02 under 510(k) number K900117. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STELLITE COBALT/CHROMIUM BASE METAL ALLOY?

STELLITE COBALT/CHROMIUM BASE METAL ALLOY is a medical device that received FDA 510(k) clearance on 1990-04-02. The listed applicant is D.C. Dental Specialties. The 510(k) number is K900117.

When did STELLITE COBALT/CHROMIUM BASE METAL ALLOY receive FDA 510(k) clearance?

STELLITE COBALT/CHROMIUM BASE METAL ALLOY received FDA 510(k) clearance on 1990-04-02, under 510(k) number K900117.

Who is the listed applicant for STELLITE COBALT/CHROMIUM BASE METAL ALLOY?

The FDA 510(k) record lists D.C. Dental Specialties as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STELLITE COBALT/CHROMIUM BASE METAL ALLOY?

The FDA product code for STELLITE COBALT/CHROMIUM BASE METAL ALLOY is EJH.

Related Clinical Trials

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.

Related Devices (Code: EJH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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