Aesculap Implant Systems, Inc.
Aesculap Implant Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2016.
Top product codes for Aesculap Implant Systems, Inc.
Recent clearances by Aesculap Implant Systems, Inc.
- K153629 — ArcadiusXP C Spinal System
- K132421 — AESCULAP PEEK XP SPINAL IMPLANT SYSTEM
- K123939 — S4 SPINAL SYSTEM
- K123352 — S4 SPINAL SYSTEM
- K111122 — AESCULAP SIBD XP SPINAL SYSTEM
- K103284 — LAMINOPLASY PLATING SYSTEM
- K100802 — AESCULAP IMPLANT SYSTEMS SIBD SPINAL SYSTEM
- K092143 — EXCIA TOTAL HIP SYSTEM M AN ML FEMORAL STEM
- K083004 — MILI (MINIMALLY INVASIVE LUMBAR IMPLANT) SYSTEM
- K083311 — AESCULAP CESPACE PEEK INTERVERTEBRAL BODY FUSION SYSTEM
- K083495 — MODIFICATION TO: METHA HIP SYSTEM
- K082991 — BIOLOX DELTA CERAMIC FEMORAL HEAD
- K081293 — UNIVATION UNICONDYLAR KNEE SYSTEM
- K082146 — METHA SHORT STEM HIP SYSTEM XL FEMORAL HEAD
- K080992 — AESCULAP IMPLANT SYSTEMS HIGH TIBIAL OSTEOTOMY PLATING SYSTEM
- K081973 — METHA SHORT STEM HIP SYSTEM; MODULAR HIP SYSTEM; EXCIA HIP SYSTEM
- K071916 — METHA HIP SYSTEM
- K071983 — AESCULAP PEEK INTERVERTEBRAL BODY FUSION SYSTEM: A SPACE, CESPACE, PROSPACE, T-SPACE
- K072899 — ORTHOPILOT 2 TOTAL HIP ARTHROPLASTY (THA) VERSION 3.0
- K071499 — COLUMBUS TOTAL KNEE SYSTEM MIOS CR/PS TIBIAL TRAY
- K070981 — SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (PLASMAPORE)
- K071220 — COLUMBUS TOTAL KNEE SYSTEM AS
Data sourced from openFDA. This site is unofficial and independent of the FDA.