The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Polyax Locked Plating System.
Device ID | K060969 |
510k Number | K060969 |
Device Name: | POLYAX LOCKED PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Contact | Rhonda Myer |
Correspondent | Rhonda Myer DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-04-07 |
Decision Date | 2006-05-12 |
Summary: | summary |