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

ATTUNE Revision Knee System

K Number: K160700 · Decision Jun 10, 2016
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
13
Review Days
88

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Basic Information

Device Name
ATTUNE Revision Knee System
K Number
K160700
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy(Ireland)
Date Received
March 14, 2016
Decision Date
June 10, 2016
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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

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Other Clearances by Depuy(Ireland)

K Number Device Name
K212683 GLOBAL ICON Stemless Shoulder System
K192855 DELTA XTEND(TM) Reverse Shoulder System
K190344 DePuy Corail AMT Hip Prosthesis
K191779 Attune Revision LPS Inserts
K192448 Delta Xtend Revers Shoulder System
K183077 Delta Xtend Reverse Shoulder System
K170806 ATTUNE Cemented Tibial Base, Fixed Bearing
K160907 DePuy Actis DuoFix Hip Prosthesis
K140881 DEPUY ATTUNE KNEE SYSTEM - CEMENTLESS CR AND PS FEMORAL COMPONENETS
K133834 DEPUY GLOBAL UNITE SHOULDER SYSTEM
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