IPW — Orthosis, Sacroiliac, Soft Class I

FDA Device Classification

FDA product code IPW covers "Orthosis, Sacroiliac, Soft", a Class I medical device regulated under 21 CFR 890.3490. Submissions are reviewed by the Physical Medicine panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
IPW
Device Class
Class I
Regulation Number
890.3490
Submission Type
Review Panel
PM
Medical Specialty
Physical Medicine
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K811176tiggsTIGGES SPINALMay 15, 1981