FDA Device Intelligence
Home › GLOBUS MEDICAL, INC. › CREO

CREO

GLOBUS MEDICAL, INC. · Model 5119.5222 · UDI-DI 00889095116519

OSHMNHNKBKWPKWQMNI
1
510(k) clearances
106
Adverse events
1
Recalls
158
Facilities

Description

CREO® Threaded 4.0 x 20mm Uniplanar Screw

Recalls

DateFirmReason
2017-08-03OrthoPediatrics CorpThe 7mm diameter uniaxial pedicle screws have been color anodized with the same color utilized on 5 mm diameter screws.

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.