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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K013676
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Product Description
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FDA Recall
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Trident Hemispherical Acetabular Shell; 72mm, Arc Deposited, Hydroxylapatite Coated, Multi holed; St... 2 08/13/2009 Stryker Howmedica Osteonics Corp.
Trident Hemispherical Acetabular Shells HA Solid BK 42mm- 74mm; Arc Deposited; Hydroxylapatite C... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident Hemispherical Cluster; 42mm - 74 mm Arc Deposited; Hydroxylapatite Coated; Multiholed; U... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident Hemispherical Multi Arc Deposited; Hydroxylapatite Coated; Multiholed; Use with Size A i... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident PSL Acetabular Shells; Trident PSL HA Solid Back, 40 mm to 73 mm, hip prosthesis component... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident PSL HA Cluster: 40 mm to 72 mm, hip prosthesis component, Stryker Orthopaedics, Howmedica ... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident Hemispherical Solid BK Acetabular Shells; 42mm to 74mm, Hydroxylapatite Coated; Multihole... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
Trident Hemispherical HA Cluster, 42 mm - 74mm Arc Deposited; Hydroxylapatite Coated; Multiholed;... 2 06/12/2008 Stryker Howmedica Osteonics Corp.
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