ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System
K-Number: K173458 · 2017-12-07
Device Summary
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. The listed applicant is Orthofix Srl. The 510(k) number is K173458.
When did ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System receive FDA 510(k) clearance?
ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System received FDA 510(k) clearance on 2017-12-07, under 510(k) number K173458.
Who is the listed applicant for ORTHOFIX CHIMAERA Hip Fracture System - Trochanteric Nailing System?
The FDA 510(k) record lists Orthofix Srl as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Orthofix Srl as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HSB)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.