meddevicedb.com FDA Device Reference

NEODYNE DRESSING

K112131 Class I Traditional
Decision Date
2011-09-29
Sponsor / Applicant
Neodyne Biosciences, Inc.

Technical Specification

510(k) Submission ID K112131
Product Code MDA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4025
Decision Date 2011-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEODYNE DRESSING received FDA 510(k) clearance under submission number K112131, sponsored by Neodyne Biosciences, 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 2011-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code MDA and 21 CFR 878.4025, within the General, Plastic Surgery review panel as a Class I device.