SIDE CUTTING SERRATED BLADE

Instrument, Cutting, Orthopedic

STAINLESS MFG., INC.

The following data is part of a premarket notification filed by Stainless Mfg., Inc. with the FDA for Side Cutting Serrated Blade.

Pre-market Notification Details

Device IDK841980
510k NumberK841980
Device Name:SIDE CUTTING SERRATED BLADE
ClassificationInstrument, Cutting, Orthopedic
Applicant STAINLESS MFG., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHTZ  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-05-14
Decision Date1984-08-15

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