meddevicedb.com FDA Device Reference

MACROSORBOS PROTECTIVE SHEET

K994158 Class II Traditional
Decision Date
2000-07-24
Sponsor / Applicant
Macropore Biosurgery, Inc.

Technical Specification

510(k) Submission ID K994158
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2000-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MACROSORBOS PROTECTIVE SHEET received FDA 510(k) clearance under submission number K994158, sponsored by Macropore Biosurgery, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-07-24.

Classification & Regulation

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