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BONE PLUGGING TOOL

K834229 Class I Traditional
Decision Date
1984-01-10
Sponsor / Applicant
Standard Surgical

Technical Specification

510(k) Submission ID K834229
Product Code HTW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4540
Decision Date 1984-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BONE PLUGGING TOOL received FDA 510(k) clearance under submission number K834229, sponsored by Standard Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1984-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code HTW and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.