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FDA 510(k)

AOS Galileo™ Trochanteric Nail System

K-Number: K202099 · 2020-08-28

ApplicantAdvanced Orthopaedic Solutions, Inc.
Decision Date2020-08-28
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AOS Galileo™ Trochanteric Nail System is a medical device manufactured by Advanced Orthopaedic Solutions, Inc.. It received FDA 510(k) clearance on 2020-08-28 under approval number K202099. 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 AOS Galileo™ Trochanteric Nail System?

AOS Galileo™ Trochanteric Nail System is a medical device that received FDA 510(k) clearance on 2020-08-28. It is manufactured by Advanced Orthopaedic Solutions, Inc.. The 510(k) number is K202099.

When was AOS Galileo™ Trochanteric Nail System approved by the FDA?

AOS Galileo™ Trochanteric Nail System received FDA 510(k) clearance on 2020-08-28, under approval number K202099.

What company makes AOS Galileo™ Trochanteric Nail System?

AOS Galileo™ Trochanteric Nail System is manufactured by Advanced Orthopaedic Solutions, Inc..

What is the FDA product code for AOS Galileo™ Trochanteric Nail System?

The FDA product code for AOS Galileo™ Trochanteric Nail System is HSB.

Other Devices by Advanced Orthopaedic Solutions, Inc.

K160409AOS Anterolateral Proximal Humeral Plate K191598AOS ES Retrograde Femoral Nail K202489AOS Fibonacci Lower Extremity Plating System – AOS Proximal Tibia Plating System

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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.

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