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FDA 510(k)

ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System

K-Number: K173458 · 2017-12-07

ApplicantOrthofix Srl
Decision Date2017-12-07
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System is a medical device manufactured by Orthofix Srl. It received FDA 510(k) clearance on 2017-12-07 under approval number K173458. 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 ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System?

ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System is a medical device that received FDA 510(k) clearance on 2017-12-07. It is manufactured by Orthofix Srl. The 510(k) number is K173458.

When was ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System approved by the FDA?

ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System received FDA 510(k) clearance on 2017-12-07, under approval number K173458.

What company makes ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System?

ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System is manufactured by Orthofix Srl.

What is the FDA product code for ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System?

The FDA product code for ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System is 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.