TUPPER TROLLEY

Apparatus, Traction, Non-powered

ORTHOPEDIC SYSTEMS, INC.

The following data is part of a premarket notification filed by Orthopedic Systems, Inc. with the FDA for Tupper Trolley.

Pre-market Notification Details

Device IDK870102
510k NumberK870102
Device Name:TUPPER TROLLEY
ClassificationApparatus, Traction, Non-powered
Applicant ORTHOPEDIC SYSTEMS, INC. 1897 NATIONAL AVE. Hayward,  CA  94545
ContactRobert R Moore
CorrespondentRobert R Moore
ORTHOPEDIC SYSTEMS, INC. 1897 NATIONAL AVE. Hayward,  CA  94545
Product CodeHST  
CFR Regulation Number888.5850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-01-09
Decision Date1987-02-03

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