Suture Nonabsorbable- Silk, Polyester

FDA 510(k) K932038 · Surgical Specialties, Inc.

Substantially Equivalent

510(k) numberK932038

Submission

Device name
Suture Nonabsorbable- Silk, Polyester
Applicant
Surgical Specialties, Inc.
Readding, PA, US
Received
April 27, 1993
Decision date
January 7, 1994
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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K254275HyperSuture All Green Extension LineGAT · Traditional Threadstone, LLC03/23/2026SE
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

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K071989Quill Self-Retaining System (SRS) Synthetic Absorbable Surgical Suture MaterialNEW · Traditional 08/06/2007SE
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Questions and answers

When was Suture Nonabsorbable- Silk, Polyester cleared by the FDA?

Suture Nonabsorbable- Silk, Polyester (K932038) received a 510(k) decision of Substantially Equivalent on January 7, 1994, 255 days after the submission was received.

What is the product code of K932038?

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