The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Ibalance Tka System.
Device ID | K152382 |
510k Number | K152382 |
Device Name: | Arthrex IBalance TKA System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | ARTHREX, INC. 1370 CREEKSIDE BOULEVARD Naples, FL 34108 -1945 |
Contact | Leon Brown |
Correspondent | Leon Brown ARTHREX, INC. 1370 CREEKSIDE BOULEVARD Naples, FL 34108 -1945 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-08-24 |
Decision Date | 2015-11-12 |
Summary: | summary |