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XANCHOR SUTURE ATTACHMENT DEVICE

K932041 Class II Traditional
Decision Date
1994-08-12
Sponsor / Applicant
Orthopaedic Biosystems

Technical Specification

510(k) Submission ID K932041
Product Code JDR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1994-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XANCHOR SUTURE ATTACHMENT DEVICE received FDA 510(k) clearance under submission number K932041, sponsored by Orthopaedic Biosystems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code JDR and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.