510(k) K223424

Spine Auto Views by GE Medical Systems SCS — Product Code JAK

K223424 is an FDA 510(k) premarket notification submitted by GE Medical Systems SCS for the device "Spine Auto Views". The FDA issued a decision of Substantially Equivalent on July 13, 2023. The device falls under product code JAK (System, X-Ray, Tomography, Computed), a Class II device regulated under 21 CFR 892.1750. GE Medical Systems SCS has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 13, 2023
Date Received
November 14, 2022
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Tomography, Computed
Device Class
Class II
Regulation Number
892.1750
Review Panel
RA
Submission Type