The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Versa-fx Femoral Fixation System, Versa-fx Ii Femoral Fixation System, Free-lock Femoral Fixation System.
Device ID | K150818 |
510k Number | K150818 |
Device Name: | Versa-Fx Femoral Fixation System, Versa-Fx II Femoral Fixation System, Free-Lock Femoral Fixation System |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Contact | Patrick Mccullagh |
Correspondent | Stephen H Mckelvey ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-27 |
Decision Date | 2015-05-01 |
Summary: | summary |