Aesculap Implant System, Inc.
FDA 510(k) medical device clearances.
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.