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LIGAFIX RESORBABLE INTERFERENCE SCREW, MODELS 30 AND 60

K050407 Class II Traditional
Decision Date
2005-11-04
Sponsor / Applicant
Sciences For Bio Materials

Technical Specification

510(k) Submission ID K050407
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2005-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIGAFIX RESORBABLE INTERFERENCE SCREW, MODELS 30 AND 60 received FDA 510(k) clearance under submission number K050407, sponsored by Sciences For Bio Materials. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2005-11-04.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.