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ACCIN HIP SYSTEM

K073068 Class II Traditional
Decision Date
2008-01-10
Sponsor / Applicant
Accelerated Innovation, LLC

Technical Specification

510(k) Submission ID K073068
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 2008-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCIN HIP SYSTEM received FDA 510(k) clearance under submission number K073068, sponsored by Accelerated Innovation, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.