FDA 510(k) Applications Submitted by CHRISTINA FLORES
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120155 |
01/18/2012 |
ARTHREX KNOTLESS SUTURETAK ANCHOR |
ARTHREX, INC. |
| K100159 |
01/20/2010 |
SMITH AND NEPHEW TWINFIX ULTRA TI SUTURE ANCHOR |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K130458 |
02/22/2013 |
KNOTLESS FIBERTAK SUTURE ANCHOR |
ARTHREX, INC. |
| K121124 |
04/13/2012 |
ARTHREX MIXING AND DELIVERY SYSTEM |
ARTHREX, INC. |
| K081098 |
04/17/2008 |
ENDOBUTTON CONTINUOUS LOOP (CL) |
SMITH & NEPHEW INC., ENDOSCOPY DIVISION |
| K171440 |
05/16/2017 |
Berkeley VC-10 Vacuum Curettage System |
Gyrus ACMI |
| K101377 |
05/17/2010 |
SMITH & NEWPHEW ULTRABRAID II SUTURE |
SMITH & NEWPHEW, INC |
| K091627 |
06/03/2009 |
SMITH & NEPHEW INSTRUMENT TRAYS |
SMITH & NEPHEW, INC. |
| K102122 |
07/29/2010 |
SMITH & NEPHEW MILTI-PURPOSE STERILIZATION TRAY MODEL 72202428 |
SMITH & NEPHEW, INC. |
| K092551 |
08/20/2009 |
SMITH & NEPHEW INSTRUMENT TRAYS |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K212643 |
08/20/2021 |
POWERSEAL Curved Jaw Sealer and Divider, Double Action |
Olympus Surgical Technologies America |
| K112990 |
10/06/2011 |
ACL TIGHTROPE,ACL TIGHTROPE DUUBLE BUNDLE |
ARTHREX, INC. |
| K093228 |
10/15/2009 |
SMITH & NEPHEW TWINFIX ULTRA PK SUTURE ANCHOR |
SMITH & NEPHEW, INC. |
| K123341 |
10/31/2012 |
ARTHREX PEC REPAIR BUTTON, ARTHREX LARGE PEC BUTTON, ARTHREX BICEPS BUTTON, ARTHREX PROXIMAL BICEPS BUTTON |
ARTHREX, INC. |
| K133381 |
11/04/2013 |
OMNI ARC MONOBLOCK HIP STEM |
OMNILIFE SCIENCE |
| K083635 |
12/08/2008 |
SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW |
SMITH & NEPHEW ENDOSCOPY, INC. |
| K093844 |
12/15/2009 |
SMITH & NEPHEW TWINFIX ULTRA HA SUTURE ANCHOR |
SMITH & NEPHEW, INC. |
| K093897 |
12/18/2009 |
SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR |
SMITH & NEPHEW INC., ENDOSCOPY DIV. |
| K093935 |
12/22/2009 |
SMITH & NEPHEW FOOTPRINT RCX PK SUTURE ANCHOR |
SMITH & NEPHEW, INC. |
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