FDA 510(k) Applications Submitted by SMITH & NEPHEW INC., ENDOSCOPY DIVISION

FDA 510(k) Number Submission Date Device Name Applicant
K081098 04/17/2008 ENDOBUTTON CONTINUOUS LOOP (CL) SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K070167 01/18/2007 ENDOBUTTON DIRECT SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K070908 04/02/2007 SMITH & NEPHEW KINSA RC SUTURE ANCHOR SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K072785 10/01/2007 TWINFIX FT PK SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K102982 10/07/2010 ENDOBUTTON DIRECT SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K121904 06/29/2012 GYNECOLOGY STERILIZATION TRAY SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K071586 06/11/2007 BIORAPTOR 2.3 PK SUTURE ANCHOR SMITH & NEPHEW INC., ENDOSCOPY DIVISION
K082215 08/06/2008 OSTEORAPTOR SUTURE ANCHOR SMITH & NEPHEW INC., ENDOSCOPY DIVISION


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