Unity Knee PS-C Tibial Insert

FDA 510(k) K240875 · Corin U.S.A. Limited

Substantially Equivalent

510(k) numberK240875

Submission

Device name
Unity Knee PS-C Tibial Insert
Applicant
Corin U.S.A. Limited
Tampa, FL, US
Received
March 29, 2024
Decision date
June 26, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3560
Specialty
Orthopedic
Implant
Yes

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K261734Klassic Infection Spacer SystemJWH · Traditional Total Joint Orthopedics, Inc.07/23/2026SE
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Questions and answers

When was Unity Knee PS-C Tibial Insert cleared by the FDA?

Unity Knee PS-C Tibial Insert (K240875) received a 510(k) decision of Substantially Equivalent on June 26, 2024, 89 days after the submission was received.

What is the product code of K240875?

The FDA product code is JWH – Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3560.