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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 the device name listed in this FDA 510(k) record. The listed applicant is Xerxes Arthopedix, LLC. It received FDA 510(k) clearance on 2023-06-15 under 510(k) 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. The listed applicant is Xerxes Arthopedix, LLC. The 510(k) number is K231109.

When did Xerxes Hip Stem receive FDA 510(k) clearance?

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

Who is the listed applicant for Xerxes Hip Stem?

The FDA 510(k) record lists Xerxes Arthopedix, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Xerxes Hip Stem?

The FDA product code for Xerxes Hip Stem is LZO.

Related Devices (Code: LZO)

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.

K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbHK252401implaFit® short stemsImplantcast GmbHK253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)Maxx Orthopedics, Inc.

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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