Osteonics Elbow Prosthesis

FDA 510(k) K861680 · Osteonics Corp.

Substantially Equivalent

510(k) numberK861680

Submission

Device name
Osteonics Elbow Prosthesis
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
May 1, 1986
Decision date
June 27, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K181307Zimmer Nexel Total Elbow, Connrad/Morrey Total ElbowJDC · Traditional Zimmer, Inc.01/28/2019SE
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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K984302Osteonics Spinal System Cylindrical Bone ScrewsMNH · Special 12/18/1998SE
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Questions and answers

When was Osteonics Elbow Prosthesis cleared by the FDA?

Osteonics Elbow Prosthesis (K861680) received a 510(k) decision of Substantially Equivalent on June 27, 1986, 57 days after the submission was received.

What is the product code of K861680?

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