510(k) K213701

Device
Exeter® X3® RimFit® Cup
Applicant
Howmedica Osteonics Corp., Dba Stryker Orthopaedics
510(k) number
K213701
Product code
JDI
Decision
Substantially Equivalent (SESE)
Decision date
2022-02-01
Date received
2021-11-24
Regulation
888.3350
Classification name
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Lin Song
Address
325 Corporate Dr. Mahwah NJ US 07430 07430

FDA Registration Numbers

Source Documents

510(k) summary PDF

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K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker Orthopaedics2024-08-02
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K233261Global Modular Replacement SystemHowmedica Osteonics Corp. A.K.A. Stryker Orthopaedics2023-12-08
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K220216C-Stem AMT LE ProsthesisDepuy Ireland UC2022-07-22
K213816MPO Hip InstrumentsMicroport Orthopedics, Inc.2022-01-05
K210842VerSys Cemented Revision/CalcarZimmer, Inc.2021-12-10
K203815ELEOS Limb Salvage System with BioGripOnkos Surgical2021-06-09
K203588ELEOS™ Limb Salvage SystemOnkos Surgical2021-02-05
K203090ELEOS Limb Salvage System featuring BIOGRIPOnkos Surgical2020-12-11
K201519PROFEMUR® GLADIATOR® Cemented Classic StemMicroport Orthopedics, Inc.2020-12-10
K193429Exeter V40 Femoral Stem, Exeter X3 RimFit CupHowmedica Osteonics Corp.2020-08-13
K191449ZCA All-Poly Acetabular CupsZimmer, Inc.2020-07-16