meddevicedb.com FDA Device Reference

DEMECAPRONE (POLIGLECAPRONE 25) SYNTHETIC MONOFILAMENT (PGCL) ABSORBABLE SUTURE

K130083 Class II Traditional
Decision Date
2013-07-17
Sponsor / Applicant
Demetech Corp.

Technical Specification

510(k) Submission ID K130083
Product Code GAM
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4493
Decision Date 2013-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEMECAPRONE (POLIGLECAPRONE 25) SYNTHETIC MONOFILAMENT (PGCL) ABSORBABLE SUTURE received FDA 510(k) clearance under submission number K130083, sponsored by Demetech Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2013-07-17.

Classification & Regulation

This clearance is catalogued under FDA product code GAM and 21 CFR 878.4493, within the General, Plastic Surgery review panel as a Class II device.