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 |