Anatomic Total Knee System
K-Number: K161414 · 2017-01-19
Device Summary
Frequently Asked Questions
What is the Anatomic Total Knee System?
Anatomic Total Knee System is a medical device that received FDA 510(k) clearance on 2017-01-19. The listed applicant is Amplitude. The 510(k) number is K161414.
When did Anatomic Total Knee System receive FDA 510(k) clearance?
Anatomic Total Knee System received FDA 510(k) clearance on 2017-01-19, under 510(k) number K161414.
Who is the listed applicant for Anatomic 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 Anatomic Total Knee System?
The FDA product code for Anatomic 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.