FDA 510(k) Applications Submitted by SMITH & NEPHEW ENDOSCOPY, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K970949 |
03/14/1997 |
SMITH & NEPHEW MIS INSTRUMENTS |
SMITH & NEPHEW ENDOSCOPY, INC. |
K971939 |
05/27/1997 |
SMITH & NEPHEW SUTURE COLLET |
SMITH & NEPHEW ENDOSCOPY, INC. |
K083635 |
12/08/2008 |
SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW |
SMITH & NEPHEW ENDOSCOPY, INC. |
K972599 |
07/14/1997 |
ACUFEX SCREW CANNULA |
SMITH & NEPHEW ENDOSCOPY, INC. |
K992396 |
07/19/1999 |
BIORCI SCREW |
SMITH & NEPHEW ENDOSCOPY, INC. |
K963901 |
09/27/1996 |
ELECTROSURGICAL PROBE |
SMITH & NEPHEW ENDOSCOPY, INC. |
K050580 |
03/07/2005 |
SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS |
SMITH & NEPHEW ENDOSCOPY, INC. |
K102660 |
09/15/2010 |
BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS |
SMITH & NEPHEW ENDOSCOPY, INC. |
K103309 |
11/10/2010 |
OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS |
SMITH & NEPHEW ENDOSCOPY, 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. |
K991500 |
04/29/1999 |
SMITH & NEPHEW SUTURE LOK |
SMITH & NEPHEW ENDOSCOPY, INC. |
K970416 |
02/04/1997 |
ACUFEX DOUBLE ARMED SUTURE NEEDLE |
SMITH & NEPHEW ENDOSCOPY, INC. |
K964935 |
12/10/1996 |
SUTURE LOCK |
SMITH & NEPHEW ENDOSCOPY, INC. |
K961649 |
04/30/1996 |
ACUFEX TIBIAL ANCHOR SCREW & SPIKED WASHER |
SMITH & NEPHEW ENDOSCOPY, INC. |
K962789 |
07/17/1996 |
SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM |
SMITH & NEPHEW ENDOSCOPY, INC. |
K964215 |
10/22/1996 |
ACUFEX MOSAICPLASTY COMPREHENSIVE SYSTEM |
SMITH & NEPHEW ENDOSCOPY, INC. |
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