Smith & Nephew Endoscopy, Inc. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Smith & Nephew Endoscopy, Inc. has 17 FDA 510(k) cleared medical devices. Based in Andover, US.
Historical record: 17 cleared submissions from 1996 to 2011. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Smith & Nephew Endoscopy, Inc. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Feb 03, 2011
OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS
Orthopedic
85d
Cleared
Dec 13, 2010
BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS
Orthopedic
89d
Cleared
Dec 17, 2009
SMITH & NEPHEW KNOTLESS INSTABILITY ANCHOR
Orthopedic
44d
Cleared
Jan 30, 2009
SMITH & NEPHEW PEEK INTERFERENCE SCREW
Orthopedic
88d
Cleared
Jan 30, 2009
SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW
Orthopedic
53d
Cleared
Oct 21, 2008
ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE
Orthopedic
89d
Cleared
Apr 20, 2005
SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS
Orthopedic
44d
Cleared
Jan 12, 2000
BIORCI SCREW
Orthopedic
177d
Cleared
Jul 14, 1999
SMITH & NEPHEW SUTURE LOK
Gastroenterology & Urology
76d
Cleared
Sep 19, 1997
ACUFEX SCREW CANNULA
Orthopedic
67d
Cleared
Aug 06, 1997
SMITH & NEPHEW SUTURE COLLET
Gastroenterology & Urology
71d
Cleared
Apr 23, 1997
SMITH & NEPHEW MIS INSTRUMENTS
General & Plastic Surgery
40d
Cleared
Apr 21, 1997
ACUFEX DOUBLE ARMED SUTURE NEEDLE
General & Plastic Surgery
76d
Cleared
Feb 25, 1997
SUTURE LOCK
General & Plastic Surgery
77d
Cleared
Dec 20, 1996
ACUFEX MOSAICPLASTY COMPREHENSIVE SYSTEM
Orthopedic
59d
Cleared
Nov 04, 1996
ELECTROSURGICAL PROBE
General & Plastic Surgery
38d
Cleared
Aug 14, 1996
SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM
General & Plastic Surgery
28d
Cleared
Jul 16, 1996
ACUFEX TIBIAL ANCHOR SCREW & SPIKED WASHER
Orthopedic
77d