The following data is part of a premarket notification filed by Zimmer Inc. with the FDA for Ncb Periprosthetic Femur Polyaxial Locking Plate System.
Device ID | K100111 |
510k Number | K100111 |
Device Name: | NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ZIMMER INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Contact | Anthony Francalanica, Rac |
Correspondent | Anthony Francalanica, Rac ZIMMER INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-01-14 |
Decision Date | 2010-04-12 |
Summary: | summary |