The following data is part of a premarket notification filed by Exactech, Inc. with the FDA for Exactech Optetrak Logic Cc.
Device ID | K150890 |
510k Number | K150890 |
Device Name: | Exactech Optetrak Logic CC |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | EXACTECH, INC. 2320 NW 66TH COURT Gainesville, FL 32653 |
Contact | Patrick Hughes |
Correspondent | Patrick Hughes EXACTECH, INC. 2320 NW 66TH COURT Gainesville, FL 32653 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-04-02 |
Decision Date | 2015-05-29 |
Summary: | summary |