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SPINAL SURGERY INSTRUMENTATION

K782061 Class II Traditional
Decision Date
1979-03-21
Sponsor / Applicant
Stuart Drug & Surgical Supply, Inc.

Technical Specification

510(k) Submission ID K782061
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 1979-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPINAL SURGERY INSTRUMENTATION received FDA 510(k) clearance under submission number K782061, sponsored by Stuart Drug & Surgical Supply, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1979-03-21.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.