The following data is part of a premarket notification filed by Encore Medical, L.p. with the FDA for Empowr Ps Knee System.
Device ID | K160342 |
510k Number | K160342 |
Device Name: | EMPOWR PS Knee System |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Encore Medical, L.P. 9800 Metric Blvd. Austin, TX 78758 |
Contact | Teffany Hutto |
Correspondent | Teffany Hutto Encore Medical, L.P. 9800 Metric Blvd. Austin, TX 78758 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-08 |
Decision Date | 2016-05-19 |
Summary: | summary |