GEG — Elevator, Surgical, General & Plastic Surgery Class I

FDA Device Classification

FDA product code GEG covers "Elevator, Surgical, General & Plastic Surgery", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel. At least 12 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GEG
Device Class
Class I
Regulation Number
878.4800
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K891894zinnanti surgical instrumentsELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSEApril 12, 1989
K891899zinnanti surgical instrumentsELEVATORS, VARIOUS TYPESApril 12, 1989
K890365kinetic medical productsSEPTUM ELEVATORFebruary 3, 1989
K890230kinetic medical productsLIGATURE NEEDLESJanuary 27, 1989
K890253kinetic medical productsSURGICAL ELEVATORJanuary 27, 1989
K872491micro-aire surgical instruments1.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSJuly 16, 1987
K870781buckman coACROMED WALLIE-HEINIG DISECTOR/ELEVATORSMarch 9, 1987
K870591military engineeringELEVATOR, COBB SPINALFebruary 26, 1987
K870126orthopedic systemsFEMUR WRENCHFebruary 3, 1987
K864421cedar surgicalRAYLOR(TM) PERIOSTEAL ELEVATORSNovember 26, 1986
K834176imm enterprisesH.R. JAKOBI SURG. INSTRUMENTS 40/41January 27, 1984
K781449orthopedic equipment coHARRINGTON SPINAL ELEVATORSeptember 27, 1978