Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ORTHOTRAK

K-Number: K890076 · 1989-02-03

ApplicantMotion Analysis Corp.
Decision Date1989-02-03
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ORTHOTRAK is the device name listed in this FDA 510(k) record. The listed applicant is Motion Analysis Corp.. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890076. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOTRAK?

ORTHOTRAK is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Motion Analysis Corp.. The 510(k) number is K890076.

When did ORTHOTRAK receive FDA 510(k) clearance?

ORTHOTRAK received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890076.

Who is the listed applicant for ORTHOTRAK?

The FDA 510(k) record lists Motion Analysis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHOTRAK?

The FDA product code for ORTHOTRAK is LXJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Motion Analysis Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K881765CTS-3060 AUTOMATED SEMEN ANALYZERK890074SPINETRAKK890075FOOTTRAK

Related Devices (Code: LXJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K192474VERAReflexion Health, Inc.K182333VeraReflexion Health, Inc.K180880DARI HealthScientific Analytics, Inc.K171547Qualisys Clinical SystemQualisys ABK173931MindMotion(TM) GOMindmaze SAK172882UINCARE HOMEUincare Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑