Serralnyl

FDA 510(k) K020146 · Serral, S.A. DE C.V.

Substantially Equivalent

510(k) numberK020146

Submission

Device name
Serralnyl
Applicant
Serral, S.A. DE C.V.
Williamsburg, VA, US
Received
January 16, 2002
Decision date
April 15, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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

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K261484Tissue Approximation SystemGAR · Special Tas Medical, Inc.06/03/2026SE
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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

More from Nashville Surgical Instruments

510(k)DeviceDecision
K033762SerralapgGAM · Traditional 03/15/2004SE
K020597SerralgutGAL · Traditional 08/14/2002SE
K020902SerralesterGAT · Traditional 05/20/2002SE
K020901SerralsilkGAP · Traditional 04/26/2002SE
K020265Serralene, Model Catalog No 1SGAW · Traditional 03/08/2002SE

Questions and answers

When was Serralnyl cleared by the FDA?

Serralnyl (K020146) received a 510(k) decision of Substantially Equivalent on April 15, 2002, 89 days after the submission was received.

What is the product code of K020146?

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