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CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC

K003028 Class II Traditional
Decision Date
2000-11-24
Sponsor / Applicant
Osteogenics Biomedical, Inc.

Technical Specification

510(k) Submission ID K003028
Product Code NBY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5035
Decision Date 2000-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC received FDA 510(k) clearance under submission number K003028, sponsored by Osteogenics Biomedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2000-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code NBY and 21 CFR 878.5035, within the General, Plastic Surgery review panel as a Class II device.