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

Integra Salto Total Ankle System

K Number: K182878 · Decision Dec 18, 2018
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
67
Applicant Total
7
Review Days
64

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Basic Information

Device Name
Integra Salto Total Ankle System
K Number
K182878
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3110
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ascension Orthopedics
Date Received
October 15, 2018
Decision Date
December 18, 2018
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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Other Clearances by Ascension Orthopedics

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K152527 Integra DigiFuse Cannulated Intramedullary Fusion System
K151459 Integra Total Ankle Replacement System
K142413 TITAN Modular Total Shoulder System