Mako Surgical Corp.
FDA 510(k) medical device clearances.
Top product codes for Mako Surgical Corp.
Recent clearances by Mako Surgical Corp.
- K260222 — Mako Total Knee Application
- K250608 — Mako Total Knee Application (3.0); Hybrid Tip Pointer
- K243751 — Mako Total Hip Application 5.0
- K242373 — Mako Shoulder Application (1.0)
- K241011 — Mako Total Knee Application
- K220930 — Restoris Multi-Compartmental Knee System
- K220459 — Mako Total Knee Application
- K193515 — Mako Total Knee Application
- K193128 — Mako Total Hip Application
- K191998 — Mako Total Hip Application, Mako Total Knee Application
- K172301 — Mako Partial Knee Application
- K172219 — Mako Total Knee Application
- K170891 — Mako Partial Knee Application
- K170581 — Mako Total Knee Application
- K170584 — Mako Partial Knee Application
- K170593 — Mako Total Hip Application
- K143752 — Total Knee Application (TKA)
- K150307 — RESTORIS Multicompartmental Knee System
- K142606 — Trident® Tritanium® PST® Acetabular Shells
- K133811 — RESTORIS POROUS PARTIAL KNEE SYSTEM
- K093425 — MAKO SURGICAL CORP ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-THA
- K091998 — ROBOTIC ARM INTERACTIVE ORTHOPEDIC SYSTEM-HIP
- K083644 — MAKO SURGICAL TACTILE GUIDANCE SYSTEM-HIP
- K081867 — MAKO SURGICAL TACTILE GUIDANCE SYSTEM VERSION 2.0
- K082088 — MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM II
- K082081 — MAKO SURGICAL CORPORATION UNICONDYLAR KNEE IMPLANT SYSTEM III
- K080368 — MAKO SURGICAL CORP. UNICONDYLAR KNEE IMPLANT SYSTEM II
- K080029 — MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM
- K072806 — MAKO SURGICAL TACTILE GUIDANCE SYSTEM (TGS)
- K073248 — MODIFICATION TO:MAKO SURGICAL UNICONDYLAR KNEE SYSTEM
- K060017 — MAKO SURGICAL UNICONDYLAR KNEE SYSTEM
- K052851 — VOYAGER LINUX WITH TACTILE GUIDANCE SYSTEM (TGS)
- K050973 — MODIFICATION TO: VOYAGER LINUX
Data sourced from openFDA. This site is unofficial and independent of the FDA.