FDA 510(k) Applications Submitted by OrthoSensor, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180459 |
02/20/2018 |
VERASENSE for Zimmer Biomet Persona |
OrthoSensor, Inc. |
| K193580 |
12/23/2019 |
VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, VERASENSE for Zimmer Biomet Persona CR |
OrthoSensor, Inc. |
| K200587 |
03/06/2020 |
VERASENSE for Exactech Equinoxe Size 38 mm, VERASENSE for Exactech Equinoxe Size 42 mm, LinkStation MINI, LinkStation MINI Evaluation Kit, VERASENSE Software Application for Shoulder |
OrthoSensor, Inc. |
| K200665 |
03/13/2020 |
VERASENSE for Stryker Triathlon |
OrthoSensor, Inc. |
| K090474 |
02/24/2009 |
ORTHOREX INTRA-OPERATIVE LOAD SENSOR |
ORTHOSENSOR, INC. |
| K150372 |
02/13/2015 |
VERASENSE Knee System |
OrthoSensor, Inc. |
| K130380 |
02/14/2013 |
ORTHOSENSOR KNEE BALANCER |
ORTHOSENSOR, INC. |
| K131767 |
06/17/2013 |
ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM |
ORTHOSENSOR, INC. |
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