The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Biomet Tibial Trays.
Device ID | K142933 |
510k Number | K142933 |
Device Name: | Biomet Tibial Trays |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | BIOMET, INC. 56 EAST BELL DR. Warsaw, IN 46581 -0587 |
Contact | Jason Heckaman |
Correspondent | Jason Heckaman BIOMET, INC. 56 EAST BELL DR. Warsaw, IN 46581 -0587 |
Product Code | JWH |
Subsequent Product Code | MBH |
Subsequent Product Code | MBV |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-10-09 |
Decision Date | 2014-12-23 |
Summary: | summary |