FDA 510(k)

Artemis Proximal Femoral Nail System

K-Number: K221489 · 2022-10-27

Decision Date2022-10-27

Product CodeHSB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Artemis Proximal Femoral Nail System is a medical device manufactured by Glw, Inc.. It received FDA 510(k) clearance on 2022-10-27 under approval number K221489. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Artemis Proximal Femoral Nail System?

Artemis Proximal Femoral Nail System is a medical device that received FDA 510(k) clearance on 2022-10-27. It is manufactured by Glw, Inc.. The 510(k) number is K221489.

When was Artemis Proximal Femoral Nail System approved by the FDA?

Artemis Proximal Femoral Nail System received FDA 510(k) clearance on 2022-10-27, under approval number K221489.

What company makes Artemis Proximal Femoral Nail System?

Artemis Proximal Femoral Nail System is manufactured by Glw, Inc..

What is the FDA product code for Artemis Proximal Femoral Nail System?

The FDA product code for Artemis Proximal Femoral Nail System is HSB.

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Other Devices by Glw, Inc.

K201379Artemis Proximal Femoral Nail System K223847CREED Cannulated Screws

Related Devices (Code: HSB)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.