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MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS

K013964 Class II Special
Decision Date
2002-01-24
Sponsor / Applicant
Cp Medical

Technical Specification

510(k) Submission ID K013964
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2002-01-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO ACCU-SPACE PLAIN GUT ABSORBABLE SEEDING SPACERS received FDA 510(k) clearance under submission number K013964, sponsored by Cp Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.