510(k) K222572

Device
FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM? & BALTEUM-ONE? Lumbar Plate System
Applicant
Dio Medical Corporation
510(k) number
K222572
Product code
KWQ
Decision
Substantially Equivalent (SESE)
Decision date
2022-10-18
Date received
2022-08-25
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

Related Records

Applicant Contact

Contact
Milan George
Address
2100 Campus Ln. Suite 100 East Norriton PA US 19403 19403

FDA Registration Numbers

Source Documents

510(k) summary PDF

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