The following data is part of a premarket notification filed by Arthrex, Inc. with the FDA for Arthrex Ibalance Patella Implant, Dome.
| Device ID | K143047 |
| 510k Number | K143047 |
| Device Name: | Arthrex IBalance Patella Implant, Dome |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | ARTHREX, INC. 1370 CREEKSIDE BOULEVARD Naples, FL 34108 -1945 |
| Contact | Laura Medlin |
| Correspondent | Laura Medlin 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 | 2014-10-23 |
| Decision Date | 2014-11-19 |
| Summary: | summary |