Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONQUEST FN

K-Number: K193029 · 2020-02-28

Decision Date2020-02-28
Product CodeJDO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONQUEST FN is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2020-02-28 under approval number K193029. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONQUEST FN?

CONQUEST FN is a medical device that received FDA 510(k) clearance on 2020-02-28. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K193029.

When was CONQUEST FN approved by the FDA?

CONQUEST FN received FDA 510(k) clearance on 2020-02-28, under approval number K193029.

What company makes CONQUEST FN?

CONQUEST FN is manufactured by Smith & Nephew, Inc..

What is the FDA product code for CONQUEST FN?

The FDA product code for CONQUEST FN is JDO.

Other Devices by Smith & Nephew, Inc.

View all 107 devices →

Related Devices (Code: JDO)

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.