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 |