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PLUS FRACTURE HEAD PROSTHESIS

K990309 Class II Traditional
Decision Date
1999-03-15
Sponsor / Applicant
Plus Orthopedics

Technical Specification

510(k) Submission ID K990309
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1999-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLUS FRACTURE HEAD PROSTHESIS received FDA 510(k) clearance under submission number K990309, sponsored by Plus Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code KWL and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.