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HTX — Rongeur Class I

FDA Device Classification

Classification Details

Product Code
HTX
Device Class
Class I
Regulation Number
888.4540
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K874954solwayMANUAL RONGEURDecember 30, 1987
K841620plastafilFRONT RADIUS CUTTERSeptember 20, 1984
K841621plastafilBACK RADIUS CUTTERSeptember 20, 1984
K780397orthopedic equipment coORTHOPEDIC FORCEPSMarch 22, 1978
K760325depuySURGICAL INSTRUMENTS, ORTHOPEDICAugust 3, 1976