Home › Seaspine Orthopedics Corporation › Laminoplasty

Laminoplasty

Seaspine Orthopedics Corporation · Model 52-2710 · UDI-DI 10889981062002

NQW Prescription

510(k) clearances

202

Adverse events

Recalls

Facilities

Description

Self Drilling Lamina Screw, Ø2.7mm x 10mm L

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 key Read 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.