meddevicedb.com FDA Device Reference

MULTIFILAMENT STAINLESS STEEL SUTURES WITH CRIMPS

K133579 Class II Traditional
Decision Date
2014-06-26
Sponsor / Applicant
Pontis Orthopaedics, LLC

Technical Specification

510(k) Submission ID K133579
Product Code MBI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2014-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTIFILAMENT STAINLESS STEEL SUTURES WITH CRIMPS received FDA 510(k) clearance under submission number K133579, sponsored by Pontis Orthopaedics, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.