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

Hintermann Series H2 Total Ankle System

K Number: K240475 · Decision Dec 2, 2024
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
67
Applicant Total
17
Review Days
286

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Basic Information

Device Name
Hintermann Series H2 Total Ankle System
K Number
K240475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3110
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vilex, LLC
Date Received
February 20, 2024
Decision Date
December 2, 2024
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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