Zimmer Segment System Trabecular Metal Proximal Tibial Component, Trabecular Metal Proximal Component, Additional Segmen

FDA 510(k) K110940 · Zimmer, Inc.

Substantially Equivalent

510(k) numberK110940

Submission

Device name
Zimmer Segment System Trabecular Metal Proximal Tibial Component, Trabecular Metal Proximal Component, Additional Segmen
Applicant
Zimmer, Inc.
Warsaw, IN, US
Received
April 4, 2011
Decision date
July 1, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3510
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Zimmer Segment System Trabecular Metal Proximal Tibial Component, Trabecular Metal Proximal Component, Additional Segmen cleared by the FDA?

Zimmer Segment System Trabecular Metal Proximal Tibial Component, Trabecular Metal Proximal Component, Additional Segmen (K110940) received a 510(k) decision of Substantially Equivalent on July 1, 2011, 88 days after the submission was received.

What is the product code of K110940?

The FDA product code is KRO – Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3510.