The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Orthofix Truelok Hexapod System (tl-hex) V2.0.
Device ID | K170650 |
510k Number | K170650 |
Device Name: | Orthofix TrueLok Hexapod System (TL-HEX) V2.0 |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | Orthofix Srl Via Delle Nazioni 9 Bussolengo, IT 37012 |
Contact | Gianluca Ricadona |
Correspondent | Cheryl Wagonar Wagoner Consulting LLC P O Box 15729 Wilmington, NC 28408 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-03 |
Decision Date | 2017-05-10 |
Summary: | summary |