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.

Device, Percutaneous Retrieval

FDA product code MMX · 28 cleared devices

Class 2 Cardiovascular
Regulation
21 CFR 870.5150
Review panel
CV
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
2002-03-12 – 2025-02-14
↑