meddevicedb.com FDA Device Reference

BOSTON SCIENTIFIC SURGICAL MESH

K081275 Class II Abbreviated
Decision Date
2008-08-27
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K081275
Product Code PAH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3300
Decision Date 2008-08-27
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOSTON SCIENTIFIC SURGICAL MESH received FDA 510(k) clearance under submission number K081275, sponsored by Boston Scientific Corp. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2008-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code PAH and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.