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)

HEFFINGTON KNEE REST

K-Number: K862925 · 1986-08-14

ApplicantLex-Ton Orthopedics
Decision Date1986-08-14
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HEFFINGTON KNEE REST is the device name listed in this FDA 510(k) record. The listed applicant is Lex-Ton Orthopedics. It received FDA 510(k) clearance on 1986-08-14 under 510(k) number K862925. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEFFINGTON KNEE REST?

HEFFINGTON KNEE REST is a medical device that received FDA 510(k) clearance on 1986-08-14. The listed applicant is Lex-Ton Orthopedics. The 510(k) number is K862925.

When did HEFFINGTON KNEE REST receive FDA 510(k) clearance?

HEFFINGTON KNEE REST received FDA 510(k) clearance on 1986-08-14, under 510(k) number K862925.

Who is the listed applicant for HEFFINGTON KNEE REST?

The FDA 510(k) record lists Lex-Ton Orthopedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEFFINGTON KNEE REST?

The FDA product code for HEFFINGTON KNEE REST is INW.

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: INW)

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.

K944308JAMES LECKEY FREE STANDERJames Leckey DesignK944307JAMES LECKEY PRONE STANDERJames Leckey DesignK943974EURO TECH MARQUISE CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK943975EURO TECH PLATINUM CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK940238TUMBLE FORMS JUNIOR TRISTANDERCamp Intl., Inc.K932231ECONOMY HI-LOW MAT TABLE #4110 THRU 4117Bailey Mfg. Co.

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.

↑