Stryker Leibinger - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Stryker Leibinger has 12 FDA 510(k) cleared medical devices. Based in Kalamazoo, US.
Historical record: 12 cleared submissions from 1999 to 2005.
Browse the FDA 510(k) cleared devices submitted by Stryker Leibinger Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Stryker Leibinger
12 devices
Cleared
Dec 16, 2005
STRYKER CUSTOM TI IMPLANT
Neurology
66d
Cleared
Apr 15, 2005
STRYKER PATIENT SPECIFIC POLYMER IMPLANT
General & Plastic Surgery
143d
Cleared
Sep 30, 2004
STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM
Dental
105d
Cleared
Mar 12, 2004
STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM
Orthopedic
65d
Cleared
Jun 02, 2003
STRYKER NAVIGATION SYSTEM-KNEE MODULE
Neurology
301d
Cleared
Jan 13, 2003
NON-INVASIVE PATIENT FIXATION SYSTEM
Radiology
90d
Cleared
Jan 08, 2002
TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM
Orthopedic
56d
Cleared
Dec 03, 2001
MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY...
Neurology
130d
Cleared
Dec 08, 2000
LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE
Dental
290d
Cleared
May 03, 2000
COLORADO MICRODISSECTION NEEDLE
General & Plastic Surgery
90d
Cleared
May 03, 2000
MOTORIZED MICRO MULTILEAF COLLIMATOR
Radiology
90d
Cleared
Sep 22, 1999
BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT
General & Plastic Surgery
153d