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AVON PATELLO-FEMORAL JOINT PROSTHESIS

K010100 Class II Traditional
Decision Date
2001-04-06
Sponsor / Applicant
Howmedica Osteonics Corp.

Technical Specification

510(k) Submission ID K010100
Product Code KRR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3540
Decision Date 2001-04-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AVON PATELLO-FEMORAL JOINT PROSTHESIS received FDA 510(k) clearance under submission number K010100, sponsored by Howmedica Osteonics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2001-04-06.

Classification & Regulation

This clearance is catalogued under FDA product code KRR and 21 CFR 888.3540, within the Orthopedic review panel as a Class II device.