FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

DePuy Actis DuoFix Hip Prosthesis

K Number: K160907 · Decision Jul 19, 2016
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
158
Applicant Total
13
Review Days
109

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Basic Information

Device Name
DePuy Actis DuoFix Hip Prosthesis
K Number
K160907
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy(Ireland)
Date Received
April 1, 2016
Decision Date
July 19, 2016
Product Code
MEH
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
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

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K170806 ATTUNE Cemented Tibial Base, Fixed Bearing
K160700 ATTUNE Revision Knee System
K140881 DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS
K133834 DEPUY GLOBAL UNITE SHOULDER SYSTEM
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