The following data is part of a premarket notification filed by Signature Orthopaedics Pty Ltd. with the FDA for Genius Total Knee System.
Device ID | K170613 |
510k Number | K170613 |
Device Name: | Genius Total Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Signature Orthopaedics Pty Ltd. 7 Sirius Road Lane Cove, AU 2066 |
Contact | Declan Brazil |
Correspondent | Declan Brazil Signature Orthopaedics Pty Ltd. 7 Sirius Road Lane Cove, AU 2066 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-01 |
Decision Date | 2017-07-17 |
Summary: | summary |