Aesculap Implant System, Inc.
Aesculap Implant System, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2014.
Top product codes for Aesculap Implant System, Inc.
Recent clearances by Aesculap Implant System, Inc.
- K142707 — AIS Odontoid Fracture Fixation System
- K142150 — AIS MODULIFT VBR SYSTEM
- K133802 — AIS MODULIFT VBR SYSTEM
- K122783 — PLASMAFIT ACETABULAR CUP AND VITELENE INSERT
- K130887 — S4C NAVIGATION INSTRUMENTS
- K123909 — AESCULAP CESPACE XP
- K130291 — S4 SPINAL SYSTEM
- K122985 — COLUMBUS REVISION KNEE SYSTEM
- K112551 — S4 SPINAL SYSTEM
- K101281 — VEGA KNEE SYSTEM
- K100147 — S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM
- K083186 — AESCULAP HYDROLIFT VBR SYSTEM
- K090375 — ORTHOPILOT NEXT GENERATION-UKA SOFTWARE, MODEL FS210
- K083772 — COLUMBUS REVISION KNEE SYSTEM
- K090354 — LAMINOPLASTY PLATING SYSTEM
- K080547 — ORTHOPILOT NEXT GENERATION, MODEL FS101-FS106
- K080584 — METHA SHORT STEM HIP SYSTEM
- K070178 — AESCULAP RESORBABLE PIN, MODEL FR735
Data sourced from openFDA. This site is unofficial and independent of the FDA.