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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: K080402
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Recall
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FDA Recall
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Turon Shoulder System Instrumentation, Turon Humeral Head Trials, DJO Surgical 2 12/22/2010 Encore Medical, Lp
Turon Shoulder System Instrumentation, Turon Pegged Glenoid Drill Guide, REF 804-25-024, DJO Surgica... 2 12/22/2010 Encore Medical, Lp
Turon Shoulder System Instrumentation, Turon Trial Pegged Glenoid, DJO Surgical 2 12/22/2010 Encore Medical, Lp
Turon Shoulder System Instrumentation, Turon Trial Humeral Neck, DJO Surgical 2 12/22/2010 Encore Medical, Lp
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