FDA.reportPublic FDA data

510(k) K233360

Device
Curiteva Thoracolumbar Plate System
Applicant
Curiteva, Inc.
510(k) number
K233360
Product code
KWQ
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-29
Date received
2023-09-29
Regulation
888.3060
Classification name
Appliance, Fixation, Spinal Intervertebral Body
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Eric Linder
Address
25127 Will Mccomb Dr., Suite 100 Tanner AL US 35671 35671

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KWQ#

510(k), Device, Applicant table
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