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)

Ergonomic Handle

K-Number: K173272 · 2018-02-09

Decision Date2018-02-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Ergonomic Handle is a medical device manufactured by Symmetry Surgical, Inc.. It received FDA 510(k) clearance on 2018-02-09 under approval number K173272. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ergonomic Handle?

Ergonomic Handle is a medical device that received FDA 510(k) clearance on 2018-02-09. It is manufactured by Symmetry Surgical, Inc.. The 510(k) number is K173272.

When was Ergonomic Handle approved by the FDA?

Ergonomic Handle received FDA 510(k) clearance on 2018-02-09, under approval number K173272.

What company makes Ergonomic Handle?

Ergonomic Handle is manufactured by Symmetry Surgical, Inc..

What is the FDA product code for Ergonomic Handle?

The FDA product code for Ergonomic Handle is GCJ.

Other Devices by Symmetry Surgical, Inc.

Related Devices (Code: GCJ)

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.