The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Persona Partial Knee System.
| Device ID | K161592 |
| 510k Number | K161592 |
| Device Name: | Persona Partial Knee System |
| Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer |
| Applicant | BIOMET, INC. 56 EAST BELL DR. Warsaw, IN 46581 |
| Contact | Nicole J. Meredith |
| Correspondent | Nicole J. Meredith BIOMET, INC. 56 EAST BELL DR. PO Box 587 Warsaw, IN 46581 |
| Product Code | HSX |
| CFR Regulation Number | 888.3520 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-06-09 |
| Decision Date | 2016-11-03 |
| Summary: | summary |