The following data is part of a premarket notification filed by Biomet Uk Ltd. with the FDA for Oxford Fixed Lateral Bearing Partial Knee Replacement (bearings / Trays).
Device ID | K133940 |
510k Number | K133940 |
Device Name: | OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (BEARINGS / TRAYS) |
Classification | Prosthesis, Knee, Femorotibial, Semi-constrained, Cemented, Metal/polymer |
Applicant | BIOMET UK LTD. 56 EAST BELL DRIVE Warsaw, IN 46581 |
Contact | Jason Heckaman |
Correspondent | Jason Heckaman BIOMET UK LTD. 56 EAST BELL DRIVE Warsaw, IN 46581 |
Product Code | HRY |
CFR Regulation Number | 888.3530 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-23 |
Decision Date | 2014-03-28 |
Summary: | summary |