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

Arthrex iBalance TKA System

K Number: K153586 · Decision Feb 19, 2016
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
348
Review Days
65

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Basic Information

Device Name
Arthrex iBalance TKA System
K Number
K153586
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
December 16, 2015
Decision Date
February 19, 2016
Product Code
MBH
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
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

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Other Clearances by Arthrex, Inc.

K Number Device Name
K253931 Arthrex Bioabsorbable PushLock Suture Anchors
K254215 Arthrex Beaming System
K252016 Arthrex Humeral Nails
K260561 Arthrex FiberTak Suture Anchor
K260405 FiberTape Button
K252196 Arthrex FibuLock Nail System
K260353 Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button
K254229 Arthrex Nano FiberTak Suture Anchor
K253713 Arthrex Variable Angle (VA) Proximal Tibia Plating System
K252807 Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates
Search all 348 clearances from Arthrex, Inc. →