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)

HEWSON LIGAMENT BUTTON

K-Number: K792004 · 1979-11-05

Decision Date1979-11-05
Product CodeKGS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HEWSON LIGAMENT BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K792004. The device is classified under product code KGS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWSON LIGAMENT BUTTON?

HEWSON LIGAMENT BUTTON is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K792004.

When did HEWSON LIGAMENT BUTTON receive FDA 510(k) clearance?

HEWSON LIGAMENT BUTTON received FDA 510(k) clearance on 1979-11-05, under 510(k) number K792004.

Who is the listed applicant for HEWSON LIGAMENT BUTTON?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEWSON LIGAMENT BUTTON?

The FDA product code for HEWSON LIGAMENT BUTTON is KGS.

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 Richard'S Medical Equip., 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 48 devices →

Related Devices (Code: KGS)

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.

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.

↑