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)

SIMMONS PLATING SYSTEM

K-Number: K910681 · 1991-10-04

Decision Date1991-10-04
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SIMMONS PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K910681. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMMONS PLATING SYSTEM?

SIMMONS PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K910681.

When did SIMMONS PLATING SYSTEM receive FDA 510(k) clearance?

SIMMONS PLATING SYSTEM received FDA 510(k) clearance on 1991-10-04, under 510(k) number K910681.

Who is the listed applicant for SIMMONS PLATING SYSTEM?

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

What is the FDA product code for SIMMONS PLATING SYSTEM?

The FDA product code for SIMMONS PLATING SYSTEM is KWQ.

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 Smith & Nephew Richards, 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 87 devices →

Related Devices (Code: KWQ)

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.

↑