FDA Device Intelligence
HomePRECISION SPINE, INC. › Reform Ti Modular

Reform Ti Modular

PRECISION SPINE, INC. · Model 39-SF-9560 · UDI-DI 00840019971386

NOKPML Prescription
1
510(k) clearances
0
Adverse events
0
Recalls
15
Facilities

Description

Modular Fenestrated Bone-Screw - 9.5 mm x 60 mm

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.