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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: K081620
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Product Description
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FDA Recall
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Depuy DELTA Xtend, Standard humeral PE Cup Dia 38/+3 STD, sterile, Depuy France; REF 130738203. T... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humerus PE Cup, Dia 38/+6 STD, sterile, Depuy France; REF 130738206. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+9 STD, sterile, Depuy France; REF 130742209. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+6 STD, sterile, Depuy France; REF 130742206. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+3 STD, sterile, Depuy France; REF 130742203. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42+6R RET, sterile, Depuy France; REF 130742106. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+9 STD, sterile, Depuy France; REF 130738209. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+6R RET, sterile, Depuy France; REF 130738106. ... 2 01/15/2009 Depuy Orthopaedics, Inc.
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