510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K991500Substantially Equivalent

Smith & Nephew Suture Lok

Smith & Nephew Endoscopy, Inc., Mansfield MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K991500 is the FDA 510(k) clearance record for SMITH & NEPHEW SUTURE LOK, a class II device, cleared for Smith & Nephew Endoscopy, Inc. on under FDA product code OCW (Endoscopic Tissue Approximation Device). FDA's definition for product code OCW reads: "To aid in endoscopically placing sutures, staples, clips, and other fastening tools through tissue". FDA records list 18 510(k) clearances for Smith & Nephew Endoscopy, Inc., from to . As of , FDA records show no recalls naming K991500.

Clearance record

Decision date
Received
(76 days to decision)
Product code
OCW Endoscopic Tissue Approximation Device
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Smith & Nephew Endoscopy, Inc. 130 Forbes Blvd., Mansfield MA
510(k) summary
Summary
Third party review
No

Clearances, product code OCW

Trailing 12 months
1 clearance under product code OCW in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OCW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260