Osteonics Total Elbow System

FDA 510(k) K980502 · Osteonics Corp.

Substantially Equivalent

510(k) numberK980502

Submission

Device name
Osteonics Total Elbow System
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
February 9, 1998
Decision date
May 5, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JDC – Prosthesis, Elbow, Constrained, Cemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3150
Specialty
Orthopedic
Implant
Yes

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K153398Comprehensive SRS/Nexel ElbowJDC · Traditional Biomet Manufacturing Corp02/03/2016SE
K150501Zimmer Nexel Total Elbow Ulnar Cement DiverterJDC · Traditional Zimmer, Inc.04/23/2015SE
K123862Zimmer Nexel Total ElbowJDC · Traditional Zimmer, Inc.03/12/2013SE
K090473Discovery Elbow - X-SmallJDC · Special Biomet Manufacturing Corp03/25/2009SE
K060696Acclaim Total Elbow SystemJDC · Special DePuy Orthopaedics, Inc.04/14/2006SE
K053189Coonrad/Morrey Total Elbow, Model 8105 SeriesJDC · Special Zimmer, Inc.12/09/2005SE
K051975Porous Coated Discovery ElbowJDC · Special Biomet, Inc.09/06/2005SE
K042664LPS Upper ExtremityJDC · Traditional Depuy, Inc.12/08/2004SE

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Questions and answers

When was Osteonics Total Elbow System cleared by the FDA?

Osteonics Total Elbow System (K980502) received a 510(k) decision of Substantially Equivalent on May 5, 1998, 85 days after the submission was received.

What is the product code of K980502?

The FDA product code is JDC – Prosthesis, Elbow, Constrained, Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3150.