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Stryker Leibinger

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133974VARIAX DISTAL RADIUS PLATING SYSTEMMarch 24, 2014
K052871STRYKER CUSTOM TI IMPLANTDecember 16, 2005
K043250STRYKER PATIENT SPECIFIC POLYMER IMPLANTApril 15, 2005
K041651STRYKER LEIBINGER SKELETAL ANCHORING SYSTEMSeptember 30, 2004
K040022STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEMMarch 12, 2004
K022579STRYKER NAVIGATION SYSTEM-KNEE MODULEJune 2, 2003
K023449NON-INVASIVE PATIENT FIXATION SYSTEMJanuary 13, 2003
K013775TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEMJanuary 8, 2002
K012380MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPYDecember 3, 2001
K000594LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATEDecember 8, 2000
K000348COLORADO MICRODISSECTION NEEDLEMay 3, 2000
K000349MOTORIZED MICRO MULTILEAF COLLIMATORMay 3, 2000
K991398BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KITSeptember 22, 1999