The following data is part of a premarket notification filed by Zimmer,inc. with the FDA for Zimmer Periarticular Plating System.
| Device ID | K150121 |
| 510k Number | K150121 |
| Device Name: | Zimmer Periarticular Plating System |
| Classification | Plate, Fixation, Bone |
| 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 | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-01-20 |
| Decision Date | 2015-02-23 |
| Summary: | summary |