Stryker Leibinger
Stryker Leibinger appears in FDA public data with 0 recalls, 13 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 24, 2014.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K133974 | VARIAX DISTAL RADIUS PLATING SYSTEM | March 24, 2014 |
| K052871 | STRYKER CUSTOM TI IMPLANT | December 16, 2005 |
| K043250 | STRYKER PATIENT SPECIFIC POLYMER IMPLANT | April 15, 2005 |
| K041651 | STRYKER LEIBINGER SKELETAL ANCHORING SYSTEM | September 30, 2004 |
| K040022 | STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM | March 12, 2004 |
| K022579 | STRYKER NAVIGATION SYSTEM-KNEE MODULE | June 2, 2003 |
| K023449 | NON-INVASIVE PATIENT FIXATION SYSTEM | January 13, 2003 |
| K013775 | TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM | January 8, 2002 |
| K012380 | MODIFICATION TO: STRYKER NAVIGATION SYSTEM, STRYKER FLUOROSCOPY SYSTEM,VIRTUAL FLUOROSCOPY | December 3, 2001 |
| K000594 | LOCKING SCREW MANDIBULAR RECONSTRUCTION PLATE | December 8, 2000 |
| K000348 | COLORADO MICRODISSECTION NEEDLE | May 3, 2000 |
| K000349 | MOTORIZED MICRO MULTILEAF COLLIMATOR | May 3, 2000 |
| K991398 | BONESOURCE HYDROXYAPATITE CEMENT (HAC) EXPANDED KIT | September 22, 1999 |