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KNEE SYSTEM, QUADRAXIAL CONSTRAINED

K781971 Class II Traditional
Decision Date
1979-04-04
Sponsor / Applicant
Hexcel Medical

Technical Specification

510(k) Submission ID K781971
Product Code KRO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3510
Decision Date 1979-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KNEE SYSTEM, QUADRAXIAL CONSTRAINED received FDA 510(k) clearance under submission number K781971, sponsored by Hexcel Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1979-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code KRO and 21 CFR 888.3510, within the Orthopedic review panel as a Class II device.