The following data is part of a premarket notification filed by Orthosensor, Inc. with the FDA for Verasense Knee System.
| Device ID | K150372 |
| 510k Number | K150372 |
| Device Name: | VERASENSE Knee System |
| Classification | Intraoperative Orthopedic Joint Assessment Aid |
| Applicant | OrthoSensor, Inc. 1855 Griffin Road, Suite A-310 Dania Beach, FL 33004 |
| Contact | Kimberlee Washburn |
| Correspondent | Deborah Johnson OrthoSensor, Inc. 1855 Griffin Road, Suite A-310 Dania Beach, FL 33004 |
| Product Code | ONN |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-02-13 |
| Decision Date | 2016-04-15 |
| Summary: | summary |