FDA.reportPublic FDA data

510(k) K243634

Device
Maxx Libertas Bipolar Hip Head (Bipolar Hip)
Applicant
Maxx Orthopedics, Inc.
510(k) number
K243634
Product code
KWY
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-25
Date received
2024-11-25
Regulation
888.3390
Classification name
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Donald Guthner
Address
2460 General Armistead Ave. Suite 100 Norristown PA US 19403 19403

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KWY#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253357b-ONE® Bipolar HeadB-One Ortho, Corp.2026-04-13
K231526CORAIL Cemented Femoral StemDepuy Ireland UC2023-12-19
K223441SpaceFlex Acetabular CupG21, S.R.L.2023-03-23
K221794Vario-Cup SystemWaldemar Link GmbH & Co. KG2022-07-20
K220492COPAL exchange G hip spacerHeraeus Medical GmbH2022-03-23
K200709Kyocera Bipolar Hip SystemKyocera Medical Technologies, Inc.2020-04-17
K192236Fitmore Hip StemZimmer GmbH2019-11-05
K191016COPAL exchange G Hip and Knee SpacersHeraeus Medical GmbH2019-11-01
K191297iNSitu Bipolar Hip SystemTheken Companies, LLC2019-09-17
K191569Implantcast ic-Bipolar Head SystemImplantcast GmbH2019-08-28
K183114Corin BiPolar-iCorin U.S.A. Limited2019-06-05
K173455SurgTech Bipolar Head SystemSurgtech, Inc.2018-06-14
K180130ELEOS™ Bipolar Acetabular SystemOnkos Surgical, Inc.2018-02-23
K16308140-42mm BiPolar Head and 22mm Femoral HeadSignature Orthopaedics Pty, Ltd.2018-01-29
K170072Fitmore® Hip StemZimmer GmbH2017-02-07