510(k) K222833

Device
Ventana? C Spinal System
Applicant
Spinal Elements, Inc.
510(k) number
K222833
Product code
ODP
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-19
Date received
2022-09-20
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Julie Lamothe
Address
3115 Melrose Dr. Suite 200 Carlsbad CA US 92010 92010

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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