meddevicedb.com FDA Device Reference

29-140 TO 29-196 VARIOUS BONE CHISELS (OSTEOTOMES,

K851788 Class I Traditional
Decision Date
1985-06-20
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851788
Product Code FZO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1985-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

29-140 TO 29-196 VARIOUS BONE CHISELS (OSTEOTOMES, received FDA 510(k) clearance under submission number K851788, sponsored by Artiberia. 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 1985-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code FZO and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.