KWE — Prosthesis, Finger, Constrained, Metal, Uncemented Class III

FDA Device Classification

Classification Details

Product Code
KWE
Device Class
Class III
Regulation Number
888.3200
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
Yes

Definition

call for pmas to be filed by 12/26/96 per 61 FR 50709 on 9/27/96