meddevicedb.com FDA Device Reference

INTRA-ARTICULATED ARTHROSCOPIC POWER SYSTEM

K854987 Class I Traditional
Decision Date
1986-02-11
Sponsor / Applicant
Richard Wolf Medical Instruments Corp.

Technical Specification

510(k) Submission ID K854987
Product Code HWE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1986-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTRA-ARTICULATED ARTHROSCOPIC POWER SYSTEM received FDA 510(k) clearance under submission number K854987, sponsored by Richard Wolf Medical Instruments Corp.. 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 1986-02-11.

Classification & Regulation

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