Medical Device Manufacturer · US , Andover , MA

Smith & Nephew Endoscopy, Inc. - FDA 510(k) Cleared Devices

18 submissions · 17 cleared · Since 1996

Total

Cleared

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.

FDA 510(k) Regulatory Record - Smith & Nephew Endoscopy, Inc.

18 devices

1-12 of 18

Cleared Feb 03, 2011

OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS

K103309 · MAI

Orthopedic · 85d

Cleared Dec 13, 2010

BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS

K102660 · MBI

Orthopedic · 89d

Cleared Dec 17, 2009

SMITH & NEPHEW KNOTLESS INSTABILITY ANCHOR

K093428 · MBI

Orthopedic · 44d

Cleared Jan 30, 2009

SMITH & NEPHEW PEEK INTERFERENCE SCREW

K083226 · MBI

Orthopedic · 88d

Cleared Jan 30, 2009

SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW

K083635 · MBI

Orthopedic · 53d

Cleared Oct 21, 2008

ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE

K082095 · HTN

Orthopedic · 89d

Cleared Apr 20, 2005

SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS

SMITH & NEPHEW SUTURE LOK

K991500 · OCW

Gastroenterology & Urology · 76d

SMITH & NEPHEW SUTURE COLLET

K971939 · OCW

Gastroenterology & Urology · 71d

Cleared Apr 23, 1997

SMITH & NEPHEW MIS INSTRUMENTS

K970949 · GCJ

General & Plastic Surgery · 40d

Smith & Nephew Endoscopy, Inc. - FDA 510(k) Cleared Devices

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