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Response BandLoc Spinal Fixation

K200097 Class II Traditional
Decision Date
2020-03-16
Sponsor / Applicant
OrthoPediatrics Corp.

Technical Specification

510(k) Submission ID K200097
Product Code OWI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3010
Decision Date 2020-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Response BandLoc Spinal Fixation received FDA 510(k) clearance under submission number K200097, 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 2020-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code OWI and 21 CFR 888.3010, within the Orthopedic review panel as a Class II device.