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 |