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FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
22
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K905514AUTOGENESIS(TM) AUTOMATORApril 2, 1991
K883888CATHSCANNER INTRAVASCULAR ULTRASONIC IMAGING SYST.December 12, 1988
K854770MARTIN LAMINAR OSTEOSYNTHESIS SYSTEMFebruary 11, 1986
K855030CHAMPY BONE PLATES & BONE SCREWSJanuary 30, 1986
K855031MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE PJanuary 21, 1986
K853916P.M. HIP-FEMORAL PROSTHESISDecember 27, 1985
K852839FREEMAN HIPOctober 29, 1985
K853418SAFTI-BRACELETSeptember 20, 1985
K852517CLS HIP PROSTHESISSeptember 18, 1985
K852699FREEMAN ACETABULAR CUPSeptember 5, 1985
K850773PM CEMENTLESS SCREW-IN ACETABULAR CUPMay 2, 1985
K844943WEILL CEMENTLESS THREADED ACETABULAR CUPMarch 18, 1985
K844482MULLER TITANIUM BACKED ACETABULAR CUP COMPONENTFebruary 19, 1985
K840150TOTAL HIP FEMORAL COMPONENTFebruary 27, 1984
K833652YASARGIL FENESTRATED ANEURYSM CLIP &January 27, 1984
K833650YASARGIL STANDARD ANEURYSM CLIP &January 18, 1984
K833717PADGETT SUCTION CANNULADecember 14, 1983
K833651CLIP APPLYING FORCEPSNovember 29, 1983
K832100PSI SURGICAL ASPIRATOROctober 4, 1983
K832302MARK I TOTAL KNEE SYS. ARTHROPLASTYAugust 16, 1983