FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Mako Total Knee Application

K Number: K260222 · Decision Feb 25, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
33
Review Days
30

Basic Information

Device Name
Mako Total Knee Application
K Number
K260222
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mako Surgical Corp.
Date Received
January 26, 2026
Decision Date
February 25, 2026
Product Code
OLO
Advisory Committee
Neurology
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OLO Orthopedic Stereotaxic Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OLO), ordered by most recent decision date.

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Other Clearances by Mako Surgical Corp.

K Number Device Name
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
Search all 33 clearances from Mako Surgical Corp. →