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PARK CITY SHOULDER POSITIONER

K910031 Class I Traditional
Decision Date
1991-01-24
Sponsor / Applicant
Orthopedic Systems, Inc.

Technical Specification

510(k) Submission ID K910031
Product Code FWZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1991-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PARK CITY SHOULDER POSITIONER received FDA 510(k) clearance under submission number K910031, sponsored by Orthopedic Systems, 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 1991-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code FWZ and 21 CFR 878.4950, within the General, Plastic Surgery review panel as a Class I device.