510(k) K242069

Device
Eminent Spine Scoliosis Deformity Pedicle Screw System
Applicant
Eminent Spine
510(k) number
K242069
Product code
NKB
Decision
Substantially Equivalent (SESE)
Decision date
2024-09-03
Date received
2024-07-15
Regulation
888.3070
Classification name
Thoracolumbosacral Pedicle Screw System
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Stephen Courtney
Address
2004 Ventura Dr. Suite 100 Plano TX US 75093 75093

FDA Registration Numbers

Source Documents

510(k) summary PDF

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