FDA.reportPublic FDA data

510(k) K243419

Device
Altus Spine Navigation System
Applicant
Altus Partners, LLC
510(k) number
K243419
Product code
OLO
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-08
Date received
2024-11-04
Regulation
882.4560
Classification name
Orthopedic Stereotaxic Instrument
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Rand Baker
Address
1340 Enterprise Dr. West Chester PA US 19380 19380

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
K262506Remex Spine Surgery Navigation - Universal InstrumentsRemex Medical Corp.2026-08-20
K261410Navbit MARQ (PRD-001-SUP (Supine Registration Kit), PRD-001-LAT (Lateral Registration Kit))Suite 201, National Innovation Centre2026-07-30
K261205SPINEART Navigation Instrument SystemSpineart SA2026-07-29
K261024TMINI Miniature Robotic SystemTHINK Surgical, Inc.2026-07-24
K262121Ion-L Navigated InstrumentsSurGenTec, LLC2026-07-24
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