meddevicedb.com FDA Device Reference

Stryker Steri-Shield 8 Surgical Hoods and Togas

K241272 Class II Traditional
Decision Date
2024-10-16
Sponsor / Applicant
Stryker Instruments

Technical Specification

510(k) Submission ID K241272
Product Code FYA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 2024-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Stryker Steri-Shield 8 Surgical Hoods and Togas received FDA 510(k) clearance under submission number K241272, sponsored by Stryker Instruments. 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 2024-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code FYA and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.