The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Biomet Orthopaedic Salvage System (oss).
| Device ID | K141331 |
| 510k Number | K141331 |
| Device Name: | BIOMET ORTHOPAEDIC SALVAGE SYSTEM (OSS) |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| Applicant | BIOMET, INC. 56 EAST BELL DRIVE PO BOX 587 Warsaw, IN 46581 |
| Contact | Tracy Bickel Johnson |
| Correspondent | Tracy Bickel Johnson BIOMET, INC. 56 EAST BELL DRIVE PO BOX 587 Warsaw, IN 46581 |
| Product Code | JDI |
| Subsequent Product Code | KRO |
| Subsequent Product Code | LPH |
| CFR Regulation Number | 888.3350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-05-21 |
| Decision Date | 2014-10-27 |
| Summary: | summary |