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BIOMET SPORTS MEDICINE STERNAL CLOSURE SYSTEM

K110039 Class II Traditional
Decision Date
2011-05-03
Sponsor / Applicant
Biomet Sports Medicine

Technical Specification

510(k) Submission ID K110039
Product Code JDQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3010
Decision Date 2011-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOMET SPORTS MEDICINE STERNAL CLOSURE SYSTEM received FDA 510(k) clearance under submission number K110039, sponsored by Biomet Sports Medicine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-05-03.

Classification & Regulation

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