C RING CLINCHER

Forceps, General & Plastic Surgery

ORTHOPEDIC EQUIPMENT CO., INC.

The following data is part of a premarket notification filed by Orthopedic Equipment Co., Inc. with the FDA for C Ring Clincher.

Pre-market Notification Details

Device IDK781446
510k NumberK781446
Device Name:C RING CLINCHER
ClassificationForceps, General & Plastic Surgery
Applicant ORTHOPEDIC EQUIPMENT CO., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeGEN  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-08-23
Decision Date1978-09-27

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