Vital Sutures, Suturex, Cirugia Peruana

FDA 510(k) K100780 · Unilene Sac

Substantially Equivalent

510(k) numberK100780

Submission

Device name
Vital Sutures, Suturex, Cirugia Peruana
Applicant
Unilene Sac
Greenwood Village, CO, US
Received
March 19, 2010
Decision date
December 14, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NEW – Suture, Surgical, Absorbable, Polydioxanone
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4840
Specialty
General, Plastic Surgery
Implant
Yes

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K252644PINION™ PDO Knotless Suture - Absorbable Poly (P-Dioxanone) Knotless Suture; PINION™…NEW · Special M/s. Meril Endo Surgery Private Limited.09/23/2025SE
K250977Suture-TOOL SystemNEW · Special Suturion AB04/28/2025SE
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More from Suturion AB

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K123034Vital Sutures Suturex Cirugia Peruana SutumedGAR · Traditional 05/28/2013SE

Questions and answers

When was Vital Sutures, Suturex, Cirugia Peruana cleared by the FDA?

Vital Sutures, Suturex, Cirugia Peruana (K100780) received a 510(k) decision of Substantially Equivalent on December 14, 2010, 270 days after the submission was received.

What is the product code of K100780?

The FDA product code is NEW – Suture, Surgical, Absorbable, Polydioxanone, a Class II (moderate risk) device regulated under 21 CFR 878.4840.