DW217 #18 CROWN/BRIDGE & DW218 #24 CERAMIC ALLOYS
K-Number: K860439 · 1986-03-20
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Device Summary
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.
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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