TRIGEN INTERTAN
K-Number: K040212 · 2004-02-20
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Device Summary
Frequently Asked Questions
What is the TRIGEN INTERTAN?
TRIGEN INTERTAN is a medical device that received FDA 510(k) clearance on 2004-02-20. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K040212.
When did TRIGEN INTERTAN receive FDA 510(k) clearance?
TRIGEN INTERTAN received FDA 510(k) clearance on 2004-02-20, under 510(k) number K040212.
Who is the listed applicant for TRIGEN INTERTAN?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIGEN INTERTAN?
The FDA product code for TRIGEN INTERTAN is JDS.
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 Smith & Nephew, 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: JDS)
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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