Instinct Plus Endoscopic Clipping Device

FDA 510(k) K212323 · Wilson-Cook Medical, Inc.

Substantially Equivalent

510(k) numberK212323

Submission

Device name
Instinct Plus Endoscopic Clipping Device
Applicant
Wilson-Cook Medical, Inc.
Winston-Salem, NC, US
Received
July 26, 2021
Decision date
August 25, 2021
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PKL – Hemostatic Metal Clip For The Gi Tract
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4400
Specialty
Gastroenterology, Urology
Implant
Yes
Life-sustaining
Yes

Clip placement within the gastrointestinal (GI) tract for the purpose of endoscopic marking, hemostasis for mucosal/sub-mucosal defects, bleeding ulcers, arteries, polyps, diverticula in the colon, prophylactic clipping, anchoring feeding tubes, supplemental closure method of luminal perforations.

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K201322Entuit Nasal Jejunal Feeding TubeKNT · Special 06/17/2020SESK
K200972Hemospray Endoscopic HemostatQAU · Traditional 06/10/2020SE
K200247Fusion Quattro Extraction BalloonGCA · Special 02/27/2020SE
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Questions and answers

When was Instinct Plus Endoscopic Clipping Device cleared by the FDA?

Instinct Plus Endoscopic Clipping Device (K212323) received a 510(k) decision of Substantially Equivalent on August 25, 2021, 30 days after the submission was received.

What is the product code of K212323?

The FDA product code is PKL – Hemostatic Metal Clip For The Gi Tract, a Class II (moderate risk) device regulated under 21 CFR 876.4400.