FDA 510(k) Applications Submitted by SMITH & NEPHEW INC., ENDOSCOPY DIV.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100159 |
01/20/2010 |
SMITH AND NEPHEW TWINFIX ULTRA TI SUTURE ANCHOR |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K092551 |
08/20/2009 |
SMITH & NEPHEW INSTRUMENT TRAYS |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K093897 |
12/18/2009 |
SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K080358 |
02/11/2008 |
PLLA, HA SCREW |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K063726 |
12/15/2006 |
PLC SUTURE ANCHOR |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K111843 |
06/29/2011 |
ACUFEX DIRECTOR APPLICATION ANATOMIC GUIDE SYSTEM |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K073551 |
12/18/2007 |
SMITH & NEPHEW INSTRUMENT TRAYS |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K093943 |
12/22/2009 |
BIOSURE SYNC TIBIAL FIXATION DEVICE, 6MM, 8MM,10MM,12MM |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K102544 |
09/03/2010 |
SMITH & NEPHEW HIP ARTHROSCOPY REPAIR INSTRUMENT TRAY |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
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