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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
510(K) Number: K112965
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Product Description
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Recall
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FDA Recall
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"***Press FT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture, HIP***N2***2009-02***CONMED LINVATEC 11311 C... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
"***PressFT***2.1 w/ One #2 (5 metric) Hi-Fi***Suture***NP211***2009-02***CONMED LINVATEC 11311 CONC... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
"***PressFT***2.1 w/ Two #0 (3.5 metric) Hi-Fi***Sutures***NP212***2009-02***CONMED LINVATEC 11311 C... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
"***PressFT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture***NP261***2009-02***CONMED LINVATEC 11311 CONC... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
"***PressFT***2.6 w/ Two #1 (4 metric) Hi-Fi***Sutures***NP262***2009-02***CONMED LINVATEC 11311 CON... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
NP211H***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach sof... 2 10/15/2012 Linvatec Corp. dba ConMed Linvatec
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