Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Porous Polyethylene Ossicular Replacement

FDA product code LBM · 2 cleared devices

Class 2 Ear, Nose, Throat
Regulation
21 CFR 874.3450
Review panel
EN
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1982-12-03 – 1982-12-03
↑