CERADIUM V NON-PRECIOUS CERAMIC ALLOY
K-Number: K993572 · 1999-12-13
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Device Summary
Frequently Asked Questions
What is the CERADIUM V NON-PRECIOUS CERAMIC ALLOY?
CERADIUM V NON-PRECIOUS CERAMIC ALLOY is a medical device that received FDA 510(k) clearance on 1999-12-13. The listed applicant is Matech, Inc.. The 510(k) number is K993572.
When did CERADIUM V NON-PRECIOUS CERAMIC ALLOY receive FDA 510(k) clearance?
CERADIUM V NON-PRECIOUS CERAMIC ALLOY received FDA 510(k) clearance on 1999-12-13, under 510(k) number K993572.
Who is the listed applicant for CERADIUM V NON-PRECIOUS CERAMIC ALLOY?
The FDA 510(k) record lists Matech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERADIUM V NON-PRECIOUS CERAMIC ALLOY?
The FDA product code for CERADIUM V NON-PRECIOUS CERAMIC 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.
Other records listing Matech, 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: 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
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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