Data / Medical devices / Posterior Cervical Screw System

Posterior Cervical Screw System (NKG): 152 FDA-registered makers in 13 countries

152 establishments in 13 countries are registered with the FDA to make Posterior Cervical Screw System (product code NKG, Class 2, 21 CFR 888.3075). 62 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 119 510(k) clearances under this code, the latest on September 17, 2026, and lists 5 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

NKG

Device class

2

Regulation

888.3075

Medical specialty

Orthopedic

Implant

Yes

Makers by country

Makers of Posterior Cervical Screw System

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated September 17, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.