The following data is part of a premarket notification filed by Biomet, Inc with the FDA for Biomet Knee Joint Replacement Prostheses.
Device ID | K171054 |
510k Number | K171054 |
Device Name: | Biomet Knee Joint Replacement Prostheses |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | Biomet, Inc 56 East Bell Drive Warsaw, IN 46581 |
Contact | Jason Heckaman |
Correspondent | Jason Heckaman Biomet, Inc 56 East Bell Drive Warsaw, IN 46581 |
Product Code | JWH |
Subsequent Product Code | HRY |
Subsequent Product Code | MBH |
Subsequent Product Code | MBV |
Subsequent Product Code | OIY |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-04-10 |
Decision Date | 2017-07-28 |
Summary: | summary |