Lukens Silk Surgical Suture

FDA 510(k) K930942 · Lukens Medical Corp.

Substantially Equivalent

510(k) numberK930942

Submission

Device name
Lukens Silk Surgical Suture
Applicant
Lukens Medical Corp.
Mahwah, NJ, US
Received
February 23, 1993
Decision date
December 17, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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K254188Meniscus VersaflexGAT · Traditional GM Dos Reis Industria e Comercio Ltda.02/19/2026SE
K253145Pre-Sutured TendonGAT · Special Rti Surgical, Inc.10/22/2025SE
K253024ProZip Knotless ImplantGAT · Special Riverpoint Medical10/16/2025SE
K252225PowerKnot High Strength SuturesGAT · Traditional Medacta International S.A.09/12/2025SE
K252201HS FiberGAT · Special Riverpoint Medical08/13/2025SE
K242201HyperSuture White/Green Extension LineGAT · Traditional Threadstone, LLC03/27/2025SE

More from Threadstone, LLC

510(k)DeviceDecision
K965162Lukens Pga, (Polyglycolic Acid) Synthetic Absorbable Surgical Suture,Coated…GAM · Traditional 02/12/1997SE
K930945Braided Polyester Surgical SutureGAT · Traditional 12/17/1993SE
K930944Lukens Surgical Gut SutureGAL · Traditional 12/17/1993SE
K930943Lukens Nylon Surgical SutureGAR · Traditional 12/17/1993SE
K930941Lukens Polypropylene Monofilament NonabsorbableGAW · Traditional 12/17/1993SE
K930940Lukens Stainless Steel Surgical SutureGAQ · Traditional 12/17/1993SE
K904535Lu-Tex IIGAS · Traditional 01/30/1991SE

Questions and answers

When was Lukens Silk Surgical Suture cleared by the FDA?

Lukens Silk Surgical Suture (K930942) received a 510(k) decision of Substantially Equivalent on December 17, 1993, 297 days after the submission was received.

What is the product code of K930942?

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