Unisilk

FDA 510(k) K042282 · United Medical Industries Co. , Ltd.

Substantially Equivalent

510(k) numberK042282

Submission

Device name
Unisilk
Applicant
United Medical Industries Co. , Ltd.
Riyadh, Central Province, SA
Received
August 24, 2004
Decision date
December 1, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GAP – Suture, Nonabsorbable, Silk
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5030
Specialty
General, Plastic Surgery
Implant
Yes

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K232355Non absorbable Surgical Silk SutureGAP · Traditional Shandong Haidike Medical Product Co., Ltd.01/16/2024SE
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K172149FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable…GAP · Special M/s. Meril Endo Surgery Private Limited.10/20/2017SE
K162396SILK Surgical SutureGAP · Traditional Teleflexmedical, Inc.11/23/2016SE
K160623FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable…GAP · Traditional M/s. Meril Endo Surgery Private Limited.05/31/2016SE
K080684Wg-Surgical Sutures with NeedleGAP · Traditional Foosin Medical Supplies, Inc.06/09/2008SE
K071111Non-Absorbable Silk SutureGAP · Traditional Arrow Intl., Inc.07/17/2007SE

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K042288UnicrylGAM · Traditional 12/27/2004SE
K042285Unicryl MNEW · Traditional 12/10/2004SE
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Questions and answers

When was Unisilk cleared by the FDA?

Unisilk (K042282) received a 510(k) decision of Substantially Equivalent on December 1, 2004, 99 days after the submission was received.

What is the product code of K042282?

The FDA product code is GAP – Suture, Nonabsorbable, Silk, a Class II (moderate risk) device regulated under 21 CFR 878.5030.