Acetabular Dome Hole Plugs

FDA 510(k) K942809 · Osteonics Corp.

Substantially Equivalent

510(k) numberK942809

Submission

Device name
Acetabular Dome Hole Plugs
Applicant
Osteonics Corp.
Allendale, NJ, US
Received
June 14, 1994
Decision date
September 20, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JDL – Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
Device class
Class III (high risk)
Regulation
21 CFR 888.3320
Specialty
Orthopedic
Implant
Yes

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K051995Profemur Renaissance Hip StemJDL · Special Wrightmedicaltechnologyinc08/22/2005SE
K051348Conserve Total Femoral HeadJDL · Traditional Wrightmedicaltechnologyinc08/19/2005SE
K042841M2A/C2A Acetabular SystemJDL · Traditional Biomet, Inc.12/21/2004SE
K041586Profemur S Hip StemJDL · Special Wrightmedicaltechnologyinc07/09/2004SE
K041114Profemur Tapered Hip StemJDL · Special Wrightmedicaltechnologyinc05/28/2004SE
K004043Metal Transcend Articulation SystemJDL · Abbreviated Wrightmedicaltechnologyinc07/13/2001SE
K950542Metal Backed Acetabular ComponentJDL · Traditional Encore Orthopedics, Inc.05/25/1995SE

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Questions and answers

When was Acetabular Dome Hole Plugs cleared by the FDA?

Acetabular Dome Hole Plugs (K942809) received a 510(k) decision of Substantially Equivalent on September 20, 1994, 98 days after the submission was received.

What is the product code of K942809?

The FDA product code is JDL – Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component), a Class III (high risk) device regulated under 21 CFR 888.3320.