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OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5

K872092 Class I Traditional
Decision Date
1987-06-23
Sponsor / Applicant
Military Engineering, Inc.

Technical Specification

510(k) Submission ID K872092
Product Code KDG
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1987-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5 received FDA 510(k) clearance under submission number K872092, sponsored by Military Engineering, Inc.. 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 1987-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code KDG and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.