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FDA product code HXG · Class 1 · Orthopedic
1,381
Registered devices
162
Adverse events
0
Recalls
1
510(k) clearances
Devices with this code
KyphPak® First Fracture Tray — MEDTRONIC SOFAMOR DANEK, INC.MEDINAUT Plus Kyphoplasty System — IMEDICOM CO., LTD.SYNTH™ PLUS BILATERAL — IMEDICOM CO., LTD.MEDINAUT Plus Kyphoplasty System — IMEDICOM CO., LTD.CPT® — Zimmer, Inc.Reef TO — Seaspine Orthopedics CorporationSYNTH™ PLUS — IMEDICOM CO., LTD.SYNTH™ PLUS — IMEDICOM CO., LTD.Choice Spine Lumbar Spacer System (SABRE™, SHARK™, HORNET™, HARPOON™) — Choice Spine, LPSYNTH™ PLUS BILATERAL — IMEDICOM CO., LTD.Made-To-Order — WRIGHT MEDICAL TECHNOLOGY, INC.AESCULAP — Aesculap AGCalix Spinal Implant System — Xtant Medical Holdings, Inc.MEDINAUT Plus Kyphoplasty System — IMEDICOM CO., LTD.BiMobile Dual Mobility System - Instruments — WALDEMAR LINK GmbH & Co. KGKYPHON Xpander II KyphoPak Tray — MEDTRONIC SOFAMOR DANEK, INC.Novo Surgical — NOVO SURGICAL, INC.Vu a-POD — Seaspine Orthopedics CorporationAnterior Cervical Interbody Fusion Device — PRECISION SPINE, INC.SQ.LINE — Aesculap AGKyphoplasty Balloon Catheter — Jiangsu Changmei Medtech Co., Ltd.Calibrate — ALPHATEC SPINE, INC.NA — Synthes GmbHRECLAIM — DEPUY (IRELAND)
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