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

Kinos Total Ankle System

K Number: K252454 · Decision Sep 3, 2025
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
67
Applicant Total
12
Review Days
30

Basic Information

Device Name
Kinos Total Ankle System
K Number
K252454
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3110
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Restor3D
Date Received
August 4, 2025
Decision Date
September 3, 2025
Product Code
HSN
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
HSN Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

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