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ORTHOPEDIATRICS PEDIFLEX FLEXIBLE NAIL SYSTEM

K082375 Class II Traditional
Decision Date
2008-10-17
Sponsor / Applicant
OrthoPediatrics Corp.

Technical Specification

510(k) Submission ID K082375
Product Code HTY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2008-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOPEDIATRICS PEDIFLEX FLEXIBLE NAIL SYSTEM received FDA 510(k) clearance under submission number K082375, sponsored by OrthoPediatrics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code HTY and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.