BONE RONGEUR, SINGLE-ACTION

Forceps, Rongeur, Surgical

KINETIC MEDICAL PRODUCTS

The following data is part of a premarket notification filed by Kinetic Medical Products with the FDA for Bone Rongeur, Single-action.

Pre-market Notification Details

Device IDK890255
510k NumberK890255
Device Name:BONE RONGEUR, SINGLE-ACTION
ClassificationForceps, Rongeur, Surgical
Applicant KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie,  PA  16509
ContactJames I Laughner
CorrespondentJames I Laughner
KINETIC MEDICAL PRODUCTS 4934 PEACH ST. Erie,  PA  16509
Product CodeEMH  
CFR Regulation Number872.4565 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-01-18
Decision Date1989-01-27

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