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