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)

ARTHROSCOPIC LEG HOLDER

K-Number: K823400 · 1982-11-29

Decision Date1982-11-29
Product Code
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC LEG HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1982-11-29 under 510(k) number K823400. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPIC LEG HOLDER?

ARTHROSCOPIC LEG HOLDER is a medical device that received FDA 510(k) clearance on 1982-11-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K823400.

When did ARTHROSCOPIC LEG HOLDER receive FDA 510(k) clearance?

ARTHROSCOPIC LEG HOLDER received FDA 510(k) clearance on 1982-11-29, under 510(k) number K823400.

Who is the listed applicant for ARTHROSCOPIC LEG HOLDER?

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

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.

Other records listing Orthopedic Systems, Inc. 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.

View all 95 devices →

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.

↑