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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K983382
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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HA Solid Back Acetabular Shell; Arc Deposited HA Coated Included Dome hole Plug; Hip prosthesis com... 2 10/25/2007 Stryker Howmedica Osteonics Corp.
Trident PSL Acetabular Shell;Arc Deposited;Hydroxylapatite Coated;Cluster Screw Holes;Howmedica Oste... 2 09/26/2007 Stryker Howmedica Osteonics Corp.
Trident PSL HA Cluster Acetabular Shell; Arc Deposited HA Coated Cluster Screw Holes. Hip prosthes... 2 10/25/2007 Stryker Howmedica Osteonics Corp.
Trident PSL HA Solid Back 50 mm Includes Dome Hole Plug Ref 540-11-50E Intended for cementless... 2 02/03/2015 Stryker Howmedica Osteonics Corp.
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