Sorbie Total Elbow System

FDA 510(k) K955099 · Wrightmedicaltechnologyinc

Substantially Equivalent

510(k) numberK955099

Submission

Device name
Sorbie Total Elbow System
Applicant
Wrightmedicaltechnologyinc
Arlington, TN, US
Received
November 7, 1995
Decision date
February 5, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JDB – Prosthesis, Elbow, Semi-Constrained, Cemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3160
Specialty
Orthopedic
Implant
Yes

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K060438RHSJDB · Traditional Tornier04/18/2006SE
K060038Sbi Radio-Capitellar ImplantJDB · Traditional Small Bone Innovations, Inc.03/30/2006SE

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Questions and answers

When was Sorbie Total Elbow System cleared by the FDA?

Sorbie Total Elbow System (K955099) received a 510(k) decision of Substantially Equivalent on February 5, 1996, 90 days after the submission was received.

What is the product code of K955099?

The FDA product code is JDB – Prosthesis, Elbow, Semi-Constrained, Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3160.