Cleared Traditional

TUPPER TROLLEY

K870102 · Orthopedic Systems, Inc. · Neurology
Feb 1987
Decision
25d
Days
Class 1
Risk

About This 510(k) Submission

K870102 is an FDA 510(k) clearance for the TUPPER TROLLEY, a Apparatus, Traction, Non-powered (Class I — General Controls, product code HST), submitted by Orthopedic Systems, Inc. (Hayward, US). The FDA issued a Cleared decision on February 3, 1987, 25 days after receiving the submission on January 9, 1987. This device falls under the Neurology review panel. Regulated under 21 CFR 888.5850.

Submission Details

510(k) Number K870102 FDA.gov
FDA Decision Cleared SESE
Date Received January 09, 1987
Decision Date February 03, 1987
Days to Decision 25 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary —

Device Classification

Product Code HST — Apparatus, Traction, Non-powered
Device Class Class I — General Controls
CFR Regulation 21 CFR 888.5850

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