Klassic Knee System Tibial Inserts, PS-Max
K-Number: K202740 · 2020-10-09
Device Summary
Frequently Asked Questions
What is the Klassic Knee System Tibial Inserts, PS-Max?
Klassic Knee System Tibial Inserts, PS-Max is a medical device that received FDA 510(k) clearance on 2020-10-09. The listed applicant is Total Joint Orthopedics, Inc.. The 510(k) number is K202740.
When did Klassic Knee System Tibial Inserts, PS-Max receive FDA 510(k) clearance?
Klassic Knee System Tibial Inserts, PS-Max received FDA 510(k) clearance on 2020-10-09, under 510(k) number K202740.
Who is the listed applicant for Klassic Knee System Tibial Inserts, PS-Max?
The FDA 510(k) record lists Total Joint Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Klassic Knee System Tibial Inserts, PS-Max?
The FDA product code for Klassic Knee System Tibial Inserts, PS-Max is JWH.
Other records listing Total Joint Orthopedics, 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: 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.