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
Class
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FDA Recall
Posting Date
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Recalling Firm
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| 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 |
| "***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 |
| "***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***2.1 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***2.1 w/ One #2 (5 metric) Hi-Fi***Suture***NP211***2009-02***CONMED LINVATEC 11311 CONC... | 2 | 10/15/2012 | Linvatec Corp. dba ConMed Linvatec |
| "***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 |
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