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KFK — Saw, Pneumatically Powered Class I

FDA Device Classification

Classification Details

Product Code
KFK
Device Class
Class I
Regulation Number
878.4820
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K893949medmark#157 EXAM LIGHTAugust 7, 1989
K894301micro surgical instrumentsMICRO-AIRE STERNUM SAW 4800August 3, 1989
K870157micro-aire surgical instrumentsOSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMERFebruary 24, 1987
K801737amscoSTERNUM SAWAugust 20, 1980