Prism Bone Cement Mixing System

FDA 510(k) K925025 · Depuy, Inc.

Substantially Equivalent

510(k) numberK925025

Submission

Device name
Prism Bone Cement Mixing System
Applicant
Depuy, Inc.
Warsaw, IN, US
Received
October 2, 1992
Decision date
January 5, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JDZ – Mixer, Cement, For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 888.4210
Specialty
Orthopedic

Other 510(k)s with product code JDZ

510(k)DeviceApplicantDecision
K934253Exactech All Poly Acetabular CupJDZ · Traditional Exactech, Inc.04/29/1994SE
K912190Stryker High Vacuum Bone Cement Mixer/Inject SystJDZ · Traditional Stryker Corp.08/29/1991SE
K892937Reusable Bowl and Spatula for Mixing Bone CementsJDZ · Traditional Dentsply Intl.06/22/1989SE
K861086Zimmer Vacuum Mixing SystemJDZ · Traditional Zimmer, Inc.04/14/1986SE
K854077Mix Evac IIJDZ · Traditional Stryker Corp.01/31/1986SN
K853310Simplex Enhancement MixerJDZ · Traditional Howmedica Corp.09/11/1985SE
K851205CementrifugeJDZ · Traditional Biodynamic Technologies, Inc.07/16/1985SE
K843219Zimmer Bone Cement Centrifugation SysJDZ · Traditional Zimmer, Inc.11/29/1984SE
K792186Howmedica Mix-Kit IIJDZ · Traditional Howmedica Corp.12/05/1979SE
K780857Mixing Bowl & Spatula, DisposableJDZ · Traditional Howmedica Corp.06/13/1978SE

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Questions and answers

When was Prism Bone Cement Mixing System cleared by the FDA?

Prism Bone Cement Mixing System (K925025) received a 510(k) decision of Substantially Equivalent on January 5, 1994, 460 days after the submission was received.

What is the product code of K925025?

The FDA product code is JDZ – Mixer, Cement, For Clinical Use, a Class I (low risk) device regulated under 21 CFR 888.4210.