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ROCKWOOD CLAVICLE PINS

K103001 Class II Traditional
Decision Date
2011-02-17
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K103001
Product Code JDW
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2011-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ROCKWOOD CLAVICLE PINS received FDA 510(k) clearance under submission number K103001, sponsored by DePuy Orthopaedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-02-17.

Classification & Regulation

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