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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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