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

Restoris Multi-Compartmental Knee System

K Number: K220930 · Decision Jun 2, 2022
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
113
Applicant Total
33
Review Days
63

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Basic Information

Device Name
Restoris Multi-Compartmental Knee System
K Number
K220930
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mako Surgical Corp.
Date Received
March 31, 2022
Decision Date
June 2, 2022
Product Code
HSX
Advisory Committee
Orthopedic
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

Similar 510(k) Clearances

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

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Other Clearances by Mako Surgical Corp.

K Number Device Name
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
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. →