Visitec Microsurgical Suture

FDA 510(k) K922530 · Visitec Co.

Substantially Equivalent

510(k) numberK922530

Submission

Device name
Visitec Microsurgical Suture
Applicant
Visitec Co.
Sarasota, FL, US
Received
May 28, 1992
Decision date
October 20, 1992
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

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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

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K945738Visiflex Ophthalmic Surgical Incise DrapeHMT · Traditional 02/14/1995SE
K945172Visitec Silicone Retinal Implants/ExplantsHQX · Traditional 01/17/1995SE
K942234Visitec Precise-PointGAP · Traditional 07/12/1994SE
K934269Fiberoptic Illuminated InstrumentsHJM · Traditional 05/17/1994SE
K940210Visitec Eye PadEFQ · Traditional 03/07/1994SE
K933872Visi-Spear Eye SpongeHOZ · Traditional 12/27/1993SE
K923972Ophthalmic Fluid Distribution SetsFPK · Traditional 11/04/1992SE
K923645Visitec Aspirating SyringeFMF · Traditional 09/30/1992SE

Questions and answers

When was Visitec Microsurgical Suture cleared by the FDA?

Visitec Microsurgical Suture (K922530) received a 510(k) decision of Substantially Equivalent on October 20, 1992, 145 days after the submission was received.

What is the product code of K922530?

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