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HTF — Curette Class I

FDA Device Classification

Classification Details

Product Code
HTF
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
K890252kinetic medical productsBONE CURETTEJanuary 27, 1989
K870778buckman coACROMED WALLIE-HEINIG CURETTESMarch 9, 1987
K841979stainless mfg4MM CUP CURRETTEJune 19, 1984