510(k) K211414

KHEIRON Spinal Fixation System by S.M.A.I.O — Product Code NKB

K211414 is an FDA 510(k) premarket notification submitted by S.M.A.I.O for the device "KHEIRON Spinal Fixation System". The FDA issued a decision of Substantially Equivalent on August 10, 2021. The device falls under product code NKB (Thoracolumbosacral Pedicle Screw System), a Class II device regulated under 21 CFR 888.3070. S.M.A.I.O has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 10, 2021
Date Received
May 6, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Thoracolumbosacral Pedicle Screw System
Device Class
Class II
Regulation Number
888.3070
Review Panel
OR
Submission Type

Intended to provide immobilization and stabilization of spinal segments in thoracic, lumbar, and sacral spine as an adjunct to fusion.