The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Locking Anatomic & Composite Plating System.
Device ID | K083843 |
510k Number | K083843 |
Device Name: | LOCKING ANATOMIC & COMPOSITE PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
Contact | Suzana Otano |
Correspondent | Suzana Otano 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 | 2008-12-24 |
Decision Date | 2009-03-20 |
Summary: | summary |