510(k) K231098

Device
LineSider® Spinal System
Applicant
Integrity Implants, Inc.
510(k) number
K231098
Product code
NKB
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-07
Date received
2023-04-18
Regulation
888.3070
Classification name
Thoracolumbosacral Pedicle Screw System
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Alexa Kamer
Address
354 Hiatt Dr. Palm Beach Gardens FL US 33418 33418

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
03662663091091LineSiderHighridge Medical, LLC2025-10-03
03662663091084LineSiderHighridge Medical, LLC2025-10-03
03662663091046LineSiderHighridge Medical, LLC2025-10-03

Other 510(k) Records For Product Code NKB

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K253966PERLA® TL Posterior Thoraco-lumbar Fixation SystemSpineart SA2026-05-01
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K254247OSTEOMNI SPINAL FIXATION SYSTEMOsteomni, Inc.2026-02-24
K253169Duet™ Spinal Fixation SystemBox Spine, LLC2026-02-23
K253545Vulcan Spinal SystemK2m, Inc.2026-02-10
K252461Swedge™ Pedicle Screw Fixation System Bezier RodSpinal Resources, Inc.2026-01-13
K253990KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O2026-01-07
K253941CD Horizon™ ModuLeX™ Spinal System (LigaMAS Head Assembly)Medtronic Sofamor Danek USA, Inc.2026-01-07