FDA Device Intelligence
Home › Paragon 28, Inc. › Phantom® Fibula Nail System

Phantom® Fibula Nail System

Paragon 28, Inc. · Model P36-970-0006 · UDI-DI 00889795137111

KIK Prescription
1
510(k) clearances
17
Adverse events
0
Recalls
114
Facilities

Description

Removal Hook, Body

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.