FDA 510(k) Applications Submitted by KATHY REDDIG

FDA 510(k) Number Submission Date Device Name Applicant
K071300 05/09/2007 MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE SMITH & NEPHEW, INC.
K082095 07/24/2008 ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE SMITH & NEPHEW ENDOSCOPY, INC.
K083226 11/03/2008 SMITH & NEPHEW PEEK INTERFERENCE SCREW SMITH & NEPHEW ENDOSCOPY, INC.
K093428 11/03/2009 SMITH & NEPHEW KNOTLESS INSTABILITY ANCHOR SMITH & NEPHEW ENDOSCOPY, INC.


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