meddevicedb.com FDA Device Reference

Implanter incl. Accessories

K211358 Class I Traditional
Decision Date
2022-11-21
Sponsor / Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.

Technical Specification

510(k) Submission ID K211358
Product Code EBW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2022-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Implanter incl. Accessories received FDA 510(k) clearance under submission number K211358, sponsored by Guilin Woodpecker Medical Instrument Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code EBW and 21 CFR 872.4200, within the Dental review panel as a Class I device.