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 |