The following data is part of a premarket notification filed by S.m.a.i.o with the FDA for Kheiron® Spinal Fixation System.
Device ID | K201659 |
510k Number | K201659 |
Device Name: | KHEIRON® Spinal Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | S.M.A.I.O 2, Place Berthe Morisot – Parc Technologique Saint-priest, FR 69800 |
Contact | Stephanie Escoffier |
Correspondent | J.d. Webb The OrthoMedix Group, Inc. 4313 W. 3800 S. West Haven, UT 84401 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-06-18 |
Decision Date | 2020-10-05 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() KHEIRON 79165301 4872495 Live/Registered |
S.M.A.I.O 2015-03-12 |