FDA.reportPublic FDA data

510(k) K262121

Device
Ion-L Navigated Instruments
Applicant
SurGenTec, LLC
510(k) number
K262121
Product code
OLO
Decision
Substantially Equivalent (SESE)
Decision date
2026-07-24
Date received
2026-06-23
Regulation
882.4560
Classification name
Orthopedic Stereotaxic Instrument
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Richard Sharp
Address
911 Clint Moore Rd. Boca Raton FL US 33487 33487

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code OLO#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K261024TMINI Miniature Robotic SystemTHINK Surgical, Inc.2026-07-24
K261113Op.n™ Spine Navigation and Robotic GuidanceEcential Robotics2026-07-22
K261852OTS HipOrtoma AB2026-07-01
K253921VERTICALE® Navigation InstrumentsSilony Medical GmbH2026-06-26
K260480VELYS™ Robotic-Assisted SolutionDepuy Ireland UC2026-06-25
K260369Dynamis Robotic Surgical SystemLEM Surgical AG2026-06-20
K261665CORUS™ Navigation System-GNProvidence Medical Technology, Inc.2026-06-18
K260571SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrumentsLife Spine, Inc.2026-06-02
K261060Navigated LLIF Impactable TrackerTyber Medical, LLC2026-05-29
K254157CROSSNAV Navigation Enabled Instruments for Disc Preparation and InterbodyMedos International SARL2026-05-26
K260329Ion-C Navigation InstrumentsSurGenTec, LLC2026-05-22
K260582ROSA® Shoulder SystemOrthosoft Inc. (d/b/a) Zimmer CAS2026-05-21
K252880Pytheas Your Guided TrajectoryPytheas Navigation Sas2026-05-11
K260011Foundation Surgical Navigated Lateral Disc Prep InstrumentsFoundation Surgical Group, Inc.2026-04-16
K254158SPINEART Navigation Instrument SystemSpineart SA2026-04-09