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SPLINTS, FINGER/TOE

K770786 Class I Traditional
Decision Date
1977-05-18
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K770786
Product Code ILH
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1977-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPLINTS, FINGER/TOE received FDA 510(k) clearance under submission number K770786, sponsored by Depuy, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1977-05-18.

Classification & Regulation

This clearance is catalogued under FDA product code ILH and 21 CFR 890.3475, within the Physical Medicine review panel as a Class I device.