Tissue Approximation System (TAS)

FDA 510(k) K220980 · Tas Medical, Inc.

Substantially Equivalent

510(k) numberK220980

Submission

Device name
Tissue Approximation System (TAS)
Applicant
Tas Medical, Inc.
San Carlos, CA, US
Received
April 4, 2022
Decision date
July 5, 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
GAR – Suture, Nonabsorbable, Synthetic, Polyamide
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5020
Specialty
General, Plastic Surgery
Implant
Yes

Other 510(k)s with product code GAR

510(k)DeviceApplicantDecision
K261484Tissue Approximation SystemGAR · Special Tas Medical, Inc.06/03/2026SE
K212888Golnit Nylon Monofilament SutureGAR · Abbreviated Antarma, LLC Dba Golnit Sutures03/31/2022SE
K212603Non Absorbable Surgical Nylon SutureGAR · Traditional Shandong Haidike Medical Product Co., Ltd.12/22/2021SE
K192420Crownjun Nylon SutureGAR · Traditional Kono Seisakusho Co., Ltd.05/29/2020SE
K161633Rexlon, RexsilGAR · Traditional Sm Eng Co., Ltd.03/02/2017SE
K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical SutureGAR · Traditional Aesculap, Inc.02/17/2016SE
K152795RiverLon (Nylon) SutureGAR · Special Riverpoint Medical10/28/2015SE
K123034Vital Sutures Suturex Cirugia Peruana SutumedGAR · Traditional Unilene Sac05/28/2013SE
K081366Kumar T-Anchors Hernia SetGAR · Traditional Nashville Surgical Instruments07/15/2008SE
K060471FSSB Nylon Surgical SuturesGAR · Abbreviated Fssb Chirurgische Nadeln GmbH07/26/2006SE

More from Fssb Chirurgische Nadeln GmbH

510(k)DeviceDecision
K261484Tissue Approximation SystemGAR · Special 06/03/2026SE

Questions and answers

When was Tissue Approximation System (TAS) cleared by the FDA?

Tissue Approximation System (TAS) (K220980) received a 510(k) decision of Substantially Equivalent on July 5, 2023, 457 days after the submission was received.

What is the product code of K220980?

The FDA product code is GAR – Suture, Nonabsorbable, Synthetic, Polyamide, a Class II (moderate risk) device regulated under 21 CFR 878.5020.