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 |