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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 27 Results
ProductCode: JDI Applicant: HOWMEDICA OSTEONICS CORP. Decision Date To: 11/27/2021
 
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uhr bipolar implants, restoration gap ii implants Howmedica Osteonics Corp., dba Stryker Orthopaedics K222632 10/21/2022
trident® ii tritanium® acetabular shells and 6.5 mm low profile hex screws Howmedica Osteonics Corp. aka Stryker Orthopaedics K161569 10/14/2016
trident® ii acetabular system Howmedica Osteonics Corp. aka Stryker Orthopaedics K171768 10/02/2017
trident screw hole plug and trident bone spike HOWMEDICA OSTEONICS CORP. K022799 11/21/2002
trident ii acetabular system Howmedica Osteonics Corp. aka Stryker Orthopaedics K191358 10/24/2019
trident all poly cup HOWMEDICA OSTEONICS CORP. K001956 12/11/2000
trident all poly cup HOWMEDICA OSTEONICS CORP. K012026 07/18/2001
super eon plus femoral stems HOWMEDICA OSTEONICS CORP. K020989 04/26/2002
restoration® modular hip system Howmedica Osteonics Corp. (aka Stryker Orthopaedics) K193233 05/27/2020
restoration® modular hip system Howmedica Osteonics Corp., dba Stryker Orthopaedics K212187 03/01/2022
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