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FDA 510(k)

DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS

K-Number: K860439 · 1986-03-20

Decision Date1986-03-20
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS is the device name listed in this FDA 510(k) record. The listed applicant is Williams Gold Refining Co., Inc.. It received FDA 510(k) clearance on 1986-03-20 under 510(k) number K860439. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS?

DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS is a medical device that received FDA 510(k) clearance on 1986-03-20. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K860439.

When did DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS receive FDA 510(k) clearance?

DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS received FDA 510(k) clearance on 1986-03-20, under 510(k) number K860439.

Who is the listed applicant for DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS?

The FDA 510(k) record lists Williams Gold Refining Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS?

The FDA product code for DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS is EJS.

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.

Other records listing Williams Gold Refining Co., Inc. as applicant

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.

View all 26 devices →

Related Devices (Code: EJS)

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

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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