Smith & Nephew Endoscopy, Inc.
Smith & Nephew Endoscopy, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2011.
Top product codes for Smith & Nephew Endoscopy, Inc.
Recent clearances by Smith & Nephew Endoscopy, Inc.
- K103309 — OSTEORAPTOR CURVED 2.3 SUTURE ANCHORS
- K102660 — BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS
- K093428 — SMITH & NEPHEW KNOTLESS INSTABILITY ANCHOR
- K083226 — SMITH & NEPHEW PEEK INTERFERENCE SCREW
- K083635 — SMITH & NEPHEW BIOSURE PK INTERFERENCE SCREW
- K082095 — ULTRASLIDE ACROMIOCLAVICULAR AND SYNDESMOTIC REPAIR DEVICE
- K050580 — SMITH & NEPHEW INTELIJET FLUID MANAGEMENT SYSTEMS
- K992396 — BIORCI SCREW
- K991500 — SMITH & NEPHEW SUTURE LOK
- K972599 — ACUFEX SCREW CANNULA
- K971939 — SMITH & NEPHEW SUTURE COLLET
- K970949 — SMITH & NEPHEW MIS INSTRUMENTS
- K970416 — ACUFEX DOUBLE ARMED SUTURE NEEDLE
- K964935 — SUTURE LOCK
- K964215 — ACUFEX MOSAICPLASTY COMPREHENSIVE SYSTEM
- K963901 — ELECTROSURGICAL PROBE
- K962789 — SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM
- K961649 — ACUFEX TIBIAL ANCHOR SCREW & SPIKED WASHER
Data sourced from openFDA. This site is unofficial and independent of the FDA.