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)

JT-1 POWERED TRACTION UNIT

K-Number: K923103 · 1992-11-09

ApplicantChirotronics, Inc.
Decision Date1992-11-09
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

JT-1 POWERED TRACTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Chirotronics, Inc.. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K923103. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JT-1 POWERED TRACTION UNIT?

JT-1 POWERED TRACTION UNIT is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Chirotronics, Inc.. The 510(k) number is K923103.

When did JT-1 POWERED TRACTION UNIT receive FDA 510(k) clearance?

JT-1 POWERED TRACTION UNIT received FDA 510(k) clearance on 1992-11-09, under 510(k) number K923103.

Who is the listed applicant for JT-1 POWERED TRACTION UNIT?

The FDA 510(k) record lists Chirotronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JT-1 POWERED TRACTION UNIT?

The FDA product code for JT-1 POWERED TRACTION UNIT is ITH.

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

Related Devices (Code: ITH)

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.

K243775True Non-Surgical Spinal Decompression System (DRX9000-SL)Excite Medical of Tampa Bay, LLCK243366DRX9000C-SL Cervical Spinal Decompression SystemExcite Medical of Tampa Bay, LLCK214037Ergo-Flex Technologies Back on Trac (BOTGEN1) and Cervi-TracErgo-Flex Technologies, LLCK222912c1TracZimmer Medizinsysteme GmbHK112074EVERYWAY TRACTION UNIT, MODEL EVER-TRAC ET-800Everyway Medical Instruments Co.,LtdK103248INTEGRITY SPINAL CARE SYSTEMIntegra Life Sciences

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.

↑