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510(k) Clearances > September 2002 510(k) Clearances Aug 7, 2009 DC 20004-1109 510(k) STATEMENT DEVICE: M2 SINGLE USE MICROKERTOME NY 12965 510(k) SUMMARY AVAILABLE FROM FDA DEVICE: SMARTSTITCH SUTURE ..... FROM FDA DEVICE: SIGN IM NAIL SURGICAL IMPLANT GENERATION NETWOR510(k) FDA 510(k) Applications Received During November, 2002 K023843 · 11/18/2002 · SMARTSTITCH M-CONNECTOR, MODEL OM-8005; K023871 · 11/20/2002 · M3046A (M2/M3/M4) COMPACT PORTABLE PATIENT MONITOR AND MP60 & MP70 Devices - medical, inc. - FDAzilla INJECTABLE CALCIUM HYDROXYLAPATITE IMPLANT FOR SOFT TISSUE AUGMENTATION ...... SMARTSTITCH ACTUATION HANDLE, MODEL OM-8500; AND SMARTSTITCH SUTURE CARTRIDGE Recall Archives 19 REASON: Sterility of dental implants may be compromised due to cracks in ...... Recall # Z-1186-06 b) ArthroCare brand OPUS Smartstitch Magnum Wire Suture FDA 510(k) Applications Received During January, 2003 K030170 · 01/17/2003 · REUSABLE SMARTSTITCH SUTURE DEVICE, .... K030238 · 01/23/2003 · BINDAZYME ANTI-MITOCHONDRIA M2 IGGAM EIA KIT · THE BINDING SITE, LTD.
 
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