The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Proximal Tibia Locking Plate Standard And Large, 3.5mm Low Profile And Multidirectional Screws.
Device ID | K090877 |
510k Number | K090877 |
Device Name: | PROXIMAL TIBIA LOCKING PLATE STANDARD AND LARGE, 3.5MM LOW PROFILE AND MULTIDIRECTIONAL SCREWS |
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 | 2009-03-31 |
Decision Date | 2009-06-26 |
Summary: | summary |