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QUESTUS POLYESTER SUTURE SOFT TISSUE ANCHOR SYSTEM

K953264 Class II Traditional
Decision Date
1995-10-20
Sponsor / Applicant
Wrightmedicaltechnologyinc

Technical Specification

510(k) Submission ID K953264
Product Code MBI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1995-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUESTUS POLYESTER SUTURE SOFT TISSUE ANCHOR SYSTEM received FDA 510(k) clearance under submission number K953264, sponsored by Wrightmedicaltechnologyinc. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1995-10-20.

Classification & Regulation

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