PATI (Protector Against Tongue Injury)

FDA 510(k) K221469 · Neurovice, LLC

Substantially Equivalent

510(k) numberK221469

Submission

Device name
PATI (Protector Against Tongue Injury)
Applicant
Neurovice, LLC
Wake Forest, NC, US
Received
May 20, 2022
Decision date
February 22, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JXL – Block, Bite
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5070
Specialty
Neurology

Other 510(k)s with product code JXL

510(k)DeviceApplicantDecision
K201309ECT Cotton Bite Block- size Large, ECT Cotton Bite Block -size MediumJXL · Traditional Mecta Corporation06/04/2021SE
K172978SurgeoBiteJXL · Traditional Surgovations, LLC12/22/2017SE
K150518Airway with Bite Block and Tongue Depressor 80 mm, Airway with Bite Block and Tongue…JXL · Traditional Dupaco, Inc.06/29/2015SE
K050188EpiguardJXL · Traditional Episafe Medical Devices, Ltd.04/27/2005SE
K992269Ventil-A Oral ProtectorJXL · Traditional Somatics, Inc.10/25/1999SE
K960663Universal Bite BlockJXL · Traditional B&B Medical Technologies, Inc.05/17/1996SE
K954352Bite BlockJXL · Traditional United States Endoscopy Group, Inc.01/25/1996SE
K941856Premier Promax Bite GuardJXL · Traditional Premier Dental Products Co.04/05/1995SE
K924333The Davis Disposable Protective SplintJXL · Traditional Ora-Gard, Inc.04/23/1993SE
K924304Bite BlockJXL · Traditional United States Endoscopy Group, Inc.04/06/1993SE

Questions and answers

When was PATI (Protector Against Tongue Injury) cleared by the FDA?

PATI (Protector Against Tongue Injury) (K221469) received a 510(k) decision of Substantially Equivalent on February 22, 2023, 278 days after the submission was received.

What is the product code of K221469?

The FDA product code is JXL – Block, Bite, a Class II (moderate risk) device regulated under 21 CFR 882.5070.