TRAX® CR Total Knee System
K-Number: K230078 · 2023-11-03
Device Summary
Frequently Asked Questions
What is the TRAX® CR Total Knee System?
TRAX® CR Total Knee System is a medical device that received FDA 510(k) clearance on 2023-11-03. The listed applicant is Amplitude. The 510(k) number is K230078.
When did TRAX® CR Total Knee System receive FDA 510(k) clearance?
TRAX® CR Total Knee System received FDA 510(k) clearance on 2023-11-03, under 510(k) number K230078.
Who is the listed applicant for TRAX® CR Total Knee System?
The FDA 510(k) record lists Amplitude as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRAX® CR Total Knee System?
The FDA product code for TRAX® CR Total Knee System is JWH.
Other records listing Amplitude 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: JWH)
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.