meddevicedb.com FDA Device Reference

Non absorbable Surgical Polypropylene Suture

K230746 Class II Traditional
Decision Date
2023-09-14
Sponsor / Applicant
Shandong Haidike Medical Products Co., Ltd.

Technical Specification

510(k) Submission ID K230746
Product Code GAW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5010
Decision Date 2023-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Non absorbable Surgical Polypropylene Suture received FDA 510(k) clearance under submission number K230746, sponsored by Shandong Haidike Medical Products Co., Ltd.. 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 2023-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code GAW and 21 CFR 878.5010, within the General, Plastic Surgery review panel as a Class II device.