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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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