'cottony' II TAPE, PLEDGETS

FDA 510(k) K153089 · Teleflexmedical, Inc.

Substantially Equivalent

510(k) numberK153089

Submission

Device name
'cottony' II TAPE, PLEDGETS
Applicant
Teleflexmedical, Inc.
Morrisville, NC, US
Received
October 26, 2015
Decision date
August 12, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GAT – Suture, Nonabsorbable, Synthetic, Polyethylene
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5000
Specialty
General, Plastic Surgery
Implant
Yes

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K252201HS FiberGAT · Special Riverpoint Medical08/13/2025SE
K242201HyperSuture White/Green Extension LineGAT · Traditional Threadstone, LLC03/27/2025SE

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Questions and answers

When was 'cottony' II TAPE, PLEDGETS cleared by the FDA?

'cottony' II TAPE, PLEDGETS (K153089) received a 510(k) decision of Substantially Equivalent on August 12, 2016, 291 days after the submission was received.

What is the product code of K153089?

The FDA product code is GAT – Suture, Nonabsorbable, Synthetic, Polyethylene, a Class II (moderate risk) device regulated under 21 CFR 878.5000.