The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Long Trochanteric Nail System.
Device ID | K013563 |
510k Number | K013563 |
Device Name: | LONG TROCHANTERIC NAIL SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DR. Warsaw, IN 46581 -0988 |
Contact | Marcia J Arentz |
Correspondent | Marcia J Arentz DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DR. Warsaw, IN 46581 -0988 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-10-26 |
Decision Date | 2001-12-27 |
Summary: | summary |