This page includes the latest FDA filings for Stryker Leibinger. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
STRYKER LEIBINGER | STRYKER CUSTOM TI IMPLANT | 2005-12-16 |
STRYKER LEIBINGER | STRYKER PATIENT SPECIFIC POLYMER IMPLANT | 2005-04-15 |
STRYKER LEIBINGER | STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM | 2004-09-30 |
STRYKER LEIBINGER | STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM | 2004-03-12 |
STRYKER LEIBINGER | STRYKER NAVIGATION SYSTEM-KNEE MODULE | 2003-06-02 |
STRYKER LEIBINGER | TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM | 2002-01-08 |
STRYKER LEIBINGER | MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY | 2001-12-03 |
STRYKER LEIBINGER | LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE | 2000-12-08 |
STRYKER LEIBINGER | MOTORIZED MICRO MULTILEAF COLLIMATOR | 2000-05-03 |
STRYKER LEIBINGER | COLORADO MICRODISSECTION NEEDLE | 2000-05-03 |
STRYKER LEIBINGER | BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT | 1999-09-22 |