The following data is part of a premarket notification filed by Encore Medical, L.p. with the FDA for Empowr Revision Knee.
Device ID | K213793 |
510k Number | K213793 |
Device Name: | EMPOWR Revision Knee |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Encore Medical, L.P. 9800 Metric Blvd. Austin, TX 78758 |
Contact | Michael Siano |
Correspondent | Michael Siano 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 | 2021-12-06 |
Decision Date | 2022-04-01 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() EMPOWR REVISION KNEE 90089641 not registered Live/Pending |
Encore Medical L.P. 2020-08-03 |