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  |