Mako Surgical Corp.
Mako Surgical Corp. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2026.
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.