The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Orthofix Chimaera Hip Fracture System - Trochanteric Nailing System.
Device ID | K161466 |
510k Number | K161466 |
Device Name: | ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | ORTHOFIX SRL VIA DELLE NAZIONI 9 Bussolengo (vr), IT 37012 |
Contact | Gianluca Ricadona |
Correspondent | Cheryl Wagoner Wagoner Consulting LLC PO Box 15729 Wilmington, NC 28408 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-05-27 |
Decision Date | 2017-01-24 |
Summary: | summary |