The following data is part of a premarket notification filed by Wright Medical Technology, Inc. with the FDA for The Inbone™ Total Ankle System, The Infinity™ Total Ankle System And The Invision™ Total Ankle Revision System.
Device ID | K193067 |
510k Number | K193067 |
Device Name: | The INBONE™ Total Ankle System, The INFINITY™ Total Ankle System And The INVISION™ Total Ankle Revision System |
Classification | Prosthesis, Ankle, Semi-constrained, Cemented, Metal/polymer |
Applicant | Wright Medical Technology, Inc. 1023 Cherry Road Memphis, TN 38117 |
Contact | Antonio Ayala |
Correspondent | Antonio Ayala Wright Medical Technology, Inc. 1023 Cherry Road Memphis, TN 38117 |
Product Code | HSN |
CFR Regulation Number | 888.3110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-11-04 |
Decision Date | 2020-06-08 |