Monoderm Surgical Suture

FDA 510(k) K140227 · Surgical Specialties Corp

Substantially Equivalent

510(k) numberK140227

Submission

Device name
Monoderm Surgical Suture
Applicant
Surgical Specialties Corp
Reading, PA, US
Received
January 30, 2014
Decision date
February 28, 2014
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GAM – Suture, Absorbable, Synthetic, Polyglycolic Acid
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4493
Specialty
General, Plastic Surgery
Implant
Yes

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K253394Coated VICRYL™ (Polyglactin 910) Plus Antibacterial SutureGAM · Traditional ETHICON, Inc.06/25/2026SE
K253530Trexon™ Monofilament Synthetic Absorbable SutureGAM · Traditional Medtronic05/28/2026SE
K253852MONOCRYL™ Plus Antibacterial Poliglecaprone – 25 (Monofilament), Sterile Synthetic…GAM · Traditional ETHICON, Inc.02/06/2026SE
K252743STRATAFIX™ Spiral PDS™ Plus Knotless Tissue Control Device; STRATAFIX™ Spiral MONOCRYL™…GAM · Traditional ETHICON, Inc.12/22/2025SE
K253620TroClose 1200GAM · Special Gordian Surgical, Ltd.12/16/2025SE
K252820PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Calypso); PGLA90…GAM · Special Internacional Farmacéutica S.A DE C.V10/03/2025SE
K233265Monotime and Optime RGAM · Abbreviated Peters Surgical10/11/2024SE
K232372Peters Surgical ADVANTIME Absorbable Suture (ADVANTIME)GAM · Abbreviated Peters Surgical07/12/2024SE
K221527StitchKitGAM · Traditional Origami Surgical Inc .02/14/2023SE
K221744STRATAFIX™ Spiral MONOCRYL™ Plus Knotless Tissue Control DeviceGAM · Traditional ETHICON, Inc.11/15/2022SE

More from ETHICON, Inc.

510(k)DeviceDecision
K160744LOOK PTFE SutureNBY · Traditional 07/13/2016SE
K141778Quill Monoderm Knotless Tissue-Closure Device, Variable Loop DesignGAM · Special 07/30/2014SE
K141625Polysyn Surgical SutureGAM · Special 07/18/2014SE
K141558Quill Monoderm Knotless Tissue-Closure DeviceGAM · Special 07/11/2014SE
K080985Quill Self-Retaining System (SRS) Comprised of Polydioxanone (Pdo)NEW · Special 04/23/2008SE
K080680Quill Self-Retaining System (SRS) Comprised of Pdo (PolydioxanoneNEW · Special 03/21/2008SE
K071989Quill Self-Retaining System (SRS) Synthetic Absorbable Surgical Suture MaterialNEW · Traditional 08/06/2007SE
K072028Quill Self-Retaining System (SRS) Comprised of MonodermGAM · Traditional 08/03/2007SE
K063680Sharpoint Pdo (Polydioxanone) SuturesNEW · Traditional 05/09/2007SE
K053380Contour Thread Synthetic Absorbable Pdo Barbed SutureNEW · Traditional 01/18/2006SE

Questions and answers

When was Monoderm Surgical Suture cleared by the FDA?

Monoderm Surgical Suture (K140227) received a 510(k) decision of Substantially Equivalent on February 28, 2014, 29 days after the submission was received.

What is the product code of K140227?

The FDA product code is GAM – Suture, Absorbable, Synthetic, Polyglycolic Acid, a Class II (moderate risk) device regulated under 21 CFR 878.4493.