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Ace Medical Surgical Instruments

K200387 Class II Traditional
Decision Date
2020-07-21
Sponsor / Applicant
Ace Medical

Technical Specification

510(k) Submission ID K200387
Product Code HAE
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4840
Decision Date 2020-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ace Medical Surgical Instruments received FDA 510(k) clearance under submission number K200387, sponsored by Ace Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2020-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code HAE and 21 CFR 882.4840, within the Neurology review panel as a Class II device.