The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Agile Nail.
Device ID | K172699 |
510k Number | K172699 |
Device Name: | Agile Nail |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | Orthofix Srl Via Delle Nazioni 9 Bussolengo, IT 37012 |
Contact | Gianluca Ricadona |
Correspondent | Cheryl Wagoner Wagoner Consulting LLC PO Box 15729 Wilmington, NC 24408 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-07 |
Decision Date | 2018-04-23 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AGILE NAIL 87637822 not registered Live/Pending |
ORTHOFIX S.R.L. 2017-10-09 |
AGILE NAIL 87619022 not registered Dead/Abandoned |
ORTHOFIX S.R.L. 2017-09-22 |