The following data is part of a premarket notification filed by Orthofix Srl with the FDA for Juniortho Plating System™.
Device ID | K213572 |
510k Number | K213572 |
Device Name: | JuniOrtho Plating System™ |
Classification | Screw, Fixation, Bone |
Applicant | Orthofix Srl Via Delle Nazioni, 9 Bussolengo, IT 37012 |
Contact | Gianluca Ricadona |
Correspondent | Cheryl Wagoner Wagoner Consulting LLG PO Box 15729 Wilmington, NC 28408 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-11-10 |
Decision Date | 2022-01-18 |