TRANSFX ANGLED RODS
K-Number: K003205 · 2000-12-15
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Device Summary
Frequently Asked Questions
What is the TRANSFX ANGLED RODS?
TRANSFX ANGLED RODS is a medical device that received FDA 510(k) clearance on 2000-12-15. The listed applicant is Immedica, Inc.. The 510(k) number is K003205.
When did TRANSFX ANGLED RODS receive FDA 510(k) clearance?
TRANSFX ANGLED RODS received FDA 510(k) clearance on 2000-12-15, under 510(k) number K003205.
Who is the listed applicant for TRANSFX ANGLED RODS?
The FDA 510(k) record lists Immedica, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRANSFX ANGLED RODS?
The FDA product code for TRANSFX ANGLED RODS is LXT.
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 Immedica, 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: LXT)
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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