Medical Device Manufacturer · US , Andover , MA

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

18 submissions · 17 cleared · Since 1996

18

Total

17

Cleared

0

Denied

FDA 510(k) Regulatory Record - Smith & Nephew Endoscopy, Inc. General & Plastic Surgery ✕

5 devices

1-5 of 5

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

General & Plastic Surgery · 77d

Cleared Nov 04, 1996

ELECTROSURGICAL PROBE

General & Plastic Surgery · 38d

Cleared Aug 14, 1996

SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM

General & Plastic Surgery · 28d