Optertrak Logic PSC Tibial Insert

FDA 510(k) K110547 · Exactech Sarasota

Substantially Equivalent

510(k) numberK110547

Submission

Device name
Optertrak Logic PSC Tibial Insert
Applicant
Exactech Sarasota
Gainesville, FL, US
Received
February 25, 2011
Decision date
April 14, 2011
Decision
Substantially Equivalent (SESE)
Type
Special 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
K261458ATTUNE Total Knee System; ATTUNE Cementless Knee SystemJWH · Traditional DePuy Ireland UC06/25/2026SE
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Questions and answers

When was Optertrak Logic PSC Tibial Insert cleared by the FDA?

Optertrak Logic PSC Tibial Insert (K110547) received a 510(k) decision of Substantially Equivalent on April 14, 2011, 48 days after the submission was received.

What is the product code of K110547?

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.