Stryker Leibinger
Stryker Leibinger holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2005.
Top product codes for Stryker Leibinger
Recent clearances by Stryker Leibinger
- K052871 — STRYKER CUSTOM TI IMPLANT
- K043250 — STRYKER PATIENT SPECIFIC POLYMER IMPLANT
- K041651 — STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM
- K040022 — STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM
- K022579 — STRYKER NAVIGATION SYSTEM-KNEE MODULE
- K023449 — NON-INVASIVE PATIENT FIXATION SYSTEM
- K013775 — TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM
- K012380 — MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY
- K000594 — LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE
- K000348 — COLORADO MICRODISSECTION NEEDLE
- K000349 — MOTORIZED MICRO MULTILEAF COLLIMATOR
- K991398 — BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.