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 |