Home › Device types › NQW
Orthosis, Spine, Plate, Laminoplasty, Metal
FDA product code NQW · Class 2 · Orthopedic
1,124
Registered devices
202
Adverse events
0
Recalls
30
510(k) clearances
Devices with this code
RELEASE® LAMINOPLASTY FIXATION SYSTEM — Pioneer Surgical Technology, Inc.Camber — Nuvasive, Inc.MOUNTAINEER — Medos International SàrlGALLERY LAMINOPLASTY SYSTEM — BIOMET SPINE LLCRELEASE® LAMINOPLASTY FIXATION SYSTEM — Pioneer Surgical Technology, Inc.Xspan Laminoplasty Fixation System — Xtant Medical Holdings, Inc.RELIEVE — GLOBUS MEDICAL, INC.RELEASE® LAMINOPLASTY FIXATION SYSTEM — Pioneer Surgical Technology, Inc.Hinged Laminoplasty — Life Spine, Inc.Xspan Laminoplasty Fixation System — Xtant Medical Holdings, Inc.Hinged Laminoplasty — Life Spine, Inc.RELEASE® LAMINOPLASTY FIXATION SYSTEM — Pioneer Surgical Technology, Inc.Xspan Laminoplasty Fixation System — Xtant Medical Holdings, Inc.Laminoplasty — Seaspine Orthopedics CorporationLaminoplasty — Seaspine Orthopedics CorporationESCALATE — Stryker CorporationHinged Laminoplasty — Life Spine, Inc.Hinged Laminoplasty — Life Spine, Inc.Xspan Laminoplasty Fixation System — Xtant Medical Holdings, Inc.RELIEVE — GLOBUS MEDICAL, INC.CANOPY — GLOBUS MEDICAL, INC.Laminoplasty — Seaspine Orthopedics CorporationLeverage — Nuvasive, Inc.CENTERPIECE™ Plate Fixation System — MEDTRONIC SOFAMOR DANEK, INC.
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.