HXL — Mallet Class I

FDA Device Classification

FDA product code HXL covers "Mallet", a Class I medical device regulated under 21 CFR 878.4800. Submissions are reviewed by the General, Plastic Surgery panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HXL
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
K882349treace medicalMALLET, SURGICALJune 23, 1988
K872209new england surgical instrumentARTHROPLASTY MALLETJune 23, 1987
K871195military engineeringMALLET, BONE SURGERY, STAINLESS STEEL, 2LB.April 6, 1987