The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Oncology Salvage System.
Device ID | K002757 |
510k Number | K002757 |
Device Name: | ONCOLOGY SALVAGE SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
Applicant | BIOMET, INC. AIRPORT INDUSTRIAL PARK, P.O.BOX 587 Warsaw, IN 46581 -0587 |
Contact | Tina Lakin |
Correspondent | Tina Lakin BIOMET, INC. AIRPORT INDUSTRIAL PARK, P.O.BOX 587 Warsaw, IN 46581 -0587 |
Product Code | JDI |
CFR Regulation Number | 888.3350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-05 |
Decision Date | 2000-11-24 |