meddevicedb.com FDA Device Reference

Non Absorbable Surgical Nylon Suture

K212603 Class II Traditional
Decision Date
2021-12-22
Sponsor / Applicant
Shandong Haidike Medical Product Co., Ltd.

Technical Specification

510(k) Submission ID K212603
Product Code GAR
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5020
Decision Date 2021-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Non Absorbable Surgical Nylon Suture received FDA 510(k) clearance under submission number K212603, sponsored by Shandong Haidike Medical Product 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 2021-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code GAR and 21 CFR 878.5020, within the General, Plastic Surgery review panel as a Class II device.