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DePuy Synthes Static Staples

K180544 Class II Traditional
Decision Date
2018-07-24
Sponsor / Applicant
Synthes (USA) Products, LLC

Technical Specification

510(k) Submission ID K180544
Product Code JDR
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2018-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DePuy Synthes Static Staples received FDA 510(k) clearance under submission number K180544, sponsored by Synthes (USA) Products, 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 2018-07-24.

Classification & Regulation

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