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)

Xerxes Hip Stem

K-Number: K231109 · 2023-06-15

ApplicantXerxes Arthopedix, LLC
Decision Date2023-06-15
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Xerxes Hip Stem is a medical device manufactured by Xerxes Arthopedix, LLC. It received FDA 510(k) clearance on 2023-06-15 under approval number K231109. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Xerxes Hip Stem?

Xerxes Hip Stem is a medical device that received FDA 510(k) clearance on 2023-06-15. It is manufactured by Xerxes Arthopedix, LLC. The 510(k) number is K231109.

When was Xerxes Hip Stem approved by the FDA?

Xerxes Hip Stem received FDA 510(k) clearance on 2023-06-15, under approval number K231109.

What company makes Xerxes Hip Stem?

Xerxes Hip Stem is manufactured by Xerxes Arthopedix, LLC.

What is the FDA product code for Xerxes Hip Stem?

The FDA product code for Xerxes Hip Stem is LZO.

Related Devices (Code: LZO)

K160895Initia Total Hip System & BIOCERAM AZUL(R) HEADKyocera Medical Corporation K161830Zimmer M/L Taper Hip ProsthesisZimmer, Inc. K161192Wagner SL Revision Stem Lateral, Wagner Cone Prosthesis® SystemZimmer GmbH K152893Corin Optimized Positioning System (OPS)Corin USA K160289MasterLoc StemMedacta International K152903REVIVAL(TM) Modular Revision Hip StemCorin USA

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.

↑