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ENSEAL PTC TISSUE SEATING SEALING DEVICE

K062949 Class II Special
Decision Date
2006-10-18
Sponsor / Applicant
Surgrx, Inc.

Technical Specification

510(k) Submission ID K062949
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2006-10-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENSEAL PTC TISSUE SEATING SEALING DEVICE received FDA 510(k) clearance under submission number K062949, sponsored by Surgrx, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2006-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.