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SPINAL SURGERY FRAME

K771020 Class I Traditional
Decision Date
1977-06-17
Sponsor / Applicant
Orthopedic Systems, Inc.

Technical Specification

510(k) Submission ID K771020
Product Code JEB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4950
Decision Date 1977-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPINAL SURGERY FRAME received FDA 510(k) clearance under submission number K771020, 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 1977-06-17.

Classification & Regulation

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