FDA.reportPublic FDA data

510(k) K792186

Device
Howmedica Mix-kit Ii
Applicant
HOWMEDICA CORP.
510(k) number
K792186
Product code
JDZ
Decision
Substantially Equivalent (SESE)
Decision date
1979-12-05
Date received
1979-10-31
Regulation
888.4210
Classification name
Mixer, Cement, For Clinical Use
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JDZ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K934253EXACTECH ALL POLY ACETABULAR CUPExactech, Inc.1994-04-29
K925025PRISM BONE CEMENT MIXING SYSTEMDepuy, Inc.1994-01-05
K912190STRYKER HIGH VACUUM BONE CEMENT MIXER/INJECT SYSTStryker Corp.1991-08-29
K892937REUSABLE BOWL AND SPATULA FOR MIXING BONE CEMENTSDentsply Intl.1989-06-22
K861086ZIMMER VACUUM MIXING SYSTEMZimmer, Inc.1986-04-14
K854077MIX EVAC IIStryker Corp.1986-01-31
K853310SIMPLEX ENHANCEMENT MIXERHowmedica Corp.1985-09-11
K851205CEMENTRIFUGEBiodynamic Technologies, Inc.1985-07-16
K843219ZIMMER BONE CEMENT CENTRIFUGATION SYSZimmer, Inc.1984-11-29
K780857MIXING BOWL & SPATULA, DISPOSABLEHowmedica Corp.1978-06-13
K760617MIX EVAC BONE CEMENTStryker Corp.1976-10-05
K760636ORTHOMIXDiemolding Corp.1976-10-05