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PREMILENE NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE

K980703 Class II Traditional
Decision Date
1998-05-04
Sponsor / Applicant
Aesculap, Inc.

Technical Specification

510(k) Submission ID K980703
Product Code GAW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5010
Decision Date 1998-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREMILENE NONABSORBABLE POLYPROPYLENE SURGICAL SUTURE received FDA 510(k) clearance under submission number K980703, sponsored by Aesculap, 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 1998-05-04.

Classification & Regulation

This clearance is catalogued under FDA product code GAW and 21 CFR 878.5010, within the General, Plastic Surgery review panel as a Class II device.