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HOWMEDICA FEMORAL PRESSURING SEAL

K811317 Class I Traditional
Decision Date
1981-05-29
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K811317
Product Code KIH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4200
Decision Date 1981-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOWMEDICA FEMORAL PRESSURING SEAL received FDA 510(k) clearance under submission number K811317, sponsored by Howmedica 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 1981-05-29.

Classification & Regulation

This clearance is catalogued under FDA product code KIH and 21 CFR 888.4200, within the Orthopedic review panel as a Class I device.