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Device Classification
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HAB — Saw, Powered, And Accessories
Class I
FDA Device Classification
Classification Details
Product Code
HAB
Device Class
Class I
Regulation Number
878.4820
Submission Type
Review Panel
SU
Medical Specialty
General, Plastic Surgery
Implant
No
Recent 510(k) Clearances
K-Number
Applicant
Device Name
Date
K012320
linvatec
POWERPRO BATTERY SYSTEM
October 19, 2001
K935517
surgiquip
SNAP STERNUM SAW
March 10, 1994