TRINON Q & Q3 IMPLANT SYSTEM
K-Number: K103577 · 2012-07-03
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Device Summary
Frequently Asked Questions
What is the TRINON Q & Q3 IMPLANT SYSTEM?
TRINON Q & Q3 IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2012-07-03. The listed applicant is Trinon Titanium GmbH. The 510(k) number is K103577.
When did TRINON Q & Q3 IMPLANT SYSTEM receive FDA 510(k) clearance?
TRINON Q & Q3 IMPLANT SYSTEM received FDA 510(k) clearance on 2012-07-03, under 510(k) number K103577.
Who is the listed applicant for TRINON Q & Q3 IMPLANT SYSTEM?
The FDA 510(k) record lists Trinon Titanium GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRINON Q & Q3 IMPLANT SYSTEM?
The FDA product code for TRINON Q & Q3 IMPLANT SYSTEM is DZE.
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 Trinon Titanium GmbH 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: DZE)
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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