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KDA — Prosthesis, Ptfe/Carbon-Fiber Class II

FDA Device Classification

Classification Details

Product Code
KDA
Device Class
Class II
Regulation Number
878.3500
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K861806medcomp technologiesMEDCARE SUTURE SCISSORS (SUTURE/GAUZE WEIGHT)May 23, 1986