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 |