FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Sapphire X3 Anterior Cervical Plate System

K Number: K231593 · Decision Aug 2, 2023
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
49
Review Days
62

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Sapphire X3 Anterior Cervical Plate System
K Number
K231593
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Elements, Inc.
Date Received
June 1, 2023
Decision Date
August 2, 2023
Product Code
KWQ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWQ), ordered by most recent decision date.

View all

Other Clearances by Spinal Elements, Inc.

K Number Device Name
K260506 Ventana® P/T Lumbar Interbody System
K253559 Ventana™ A Anterior Lumbar Interbody System
K250773 Luna® Ti Interbody Fusion System
K242527 The Karma® Fixation System
K243916 Primus Spinal Fixation System
K231252 Ventana™ L Spinal System
K222833 Ventana™ C Spinal System
K222516 Mercury® II Spinal System
K210044 Crystal Spinal System & Vertu Spinal System, Lucent Spinal System, Zeus Spinal System, Ceres-C Spinal System, Omega XP Spinal System
K203254 Lucent 3D Spinal System
Search all 49 clearances from Spinal Elements, Inc. →