meddevicedb.com FDA Device Reference

MEDICAL PLATES, LATERAL PLATES, POSTERIOR LATERAL PLATES, OLECRANON PLATES MODEL 131218704-708; 851318704-708, 131218204

K101421 Class II Special
Decision Date
2010-06-15
Sponsor / Applicant
DePuy Orthopaedics, Inc.

Technical Specification

510(k) Submission ID K101421
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2010-06-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDICAL PLATES, LATERAL PLATES, POSTERIOR LATERAL PLATES, OLECRANON PLATES MODEL 131218704-708; 851318704-708, 131218204 received FDA 510(k) clearance under submission number K101421, sponsored by DePuy Orthopaedics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2010-06-15.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.