Sharpoint Polypropylene Nonabsorb Surg Sutures Usp

FDA 510(k) K904906 · Chathamborough Research Group, Inc.

Substantially Equivalent

510(k) numberK904906

Submission

Device name
Sharpoint Polypropylene Nonabsorb Surg Sutures Usp
Applicant
Chathamborough Research Group, Inc.
Pittsboro, NC, US
Received
October 25, 1990
Decision date
December 24, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GAW – Suture, Nonabsorbable, Synthetic, Polypropylene
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5010
Specialty
General, Plastic Surgery
Implant
Yes

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K230746Non absorbable Surgical Polypropylene SutureGAW · Traditional Shandong Haidike Medical Products Co., Ltd.09/14/2023SE
K221280VessealGAW · Traditional Lydus Medical , Ltd.12/09/2022SE
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K192953APTOS Threads – Polypropylene Surgical SuturesGAW · Traditional Aptos, LLC08/27/2020SE
K193530Deklene MAXXGAW · Special Teleflex Medical03/19/2020SE
K191299Silhouette Featherlift / Silhouette LiftGAW · Special Silhouette Lift, Inc.06/14/2019SE
K173747RexleneGAW · Traditional Sm Eng Co., Ltd.12/21/2018SE
K180321Aesculap Optilene Nonabsorbable SutureGAW · Special Aesculap, Inc.03/07/2018SE

More from Aesculap, Inc.

510(k)DeviceDecision
K915676Splatter ShieldFMF · Traditional 09/11/1992SE
K902309Parker Micropump Model 2100FRN · Traditional 08/17/1990SE
K863034Sharpoint Stainless Steel SutureGAO · Traditional 09/30/1986SE

Questions and answers

When was Sharpoint Polypropylene Nonabsorb Surg Sutures Usp cleared by the FDA?

Sharpoint Polypropylene Nonabsorb Surg Sutures Usp (K904906) received a 510(k) decision of Substantially Equivalent on December 24, 1990, 60 days after the submission was received.

What is the product code of K904906?

The FDA product code is GAW – Suture, Nonabsorbable, Synthetic, Polypropylene, a Class II (moderate risk) device regulated under 21 CFR 878.5010.