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Trousers, Anti-Shock
FDA product code LHX · Class 2 · Cardiovascular
190
Registered devices
102
Adverse events
1
Recalls
4
510(k) clearances
Devices with this code
PROPHECY INBONE — WRIGHT MEDICAL TECHNOLOGY, INC.PRIMA — LIMACORPORATE SPAOrthoPediatrics PediFoot Deformity Correction System — ORTHOPEDIATRICS CORP.ALEUTIAN Interbody Systems — VB Spine LLCALEUTIAN Interbody Systems — VB Spine LLCR3 — Smith & Nephew, Inc.Salto Talaris® — Ascension Orthopedics, Inc.SMR Shoulder — LIMACORPORATE SPAPRIMA — LIMACORPORATE SPAPRIMA — LIMACORPORATE SPAGuide Pin, 2.8mm Threaded — CURVAFIX, INC.PRIMA — LIMACORPORATE SPASurgical Instruments — Smith & Nephew, Inc.ALEUTIAN Interbody Systems — VB Spine LLCOrthoPediatrics PediFoot Deformity Correction System — ORTHOPEDIATRICS CORP.ALEUTIAN Interbody Systems — VB Spine LLCALEUTIAN Interbody Systems — VB Spine LLCSpecials — Seaspine Orthopedics CorporationPaeon Posterior Cervical Fixation System — Aegis Spine, Inc.Legion — Smith & Nephew, Inc.PRIMA — LIMACORPORATE SPAPRIMA — LIMACORPORATE SPACADENCE® — Ascension Orthopedics, Inc.PRIMA — LIMACORPORATE SPA
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-01-18 | Stryker Spine | Stryker Spine received reports of packaging failures during shipping for the Jam Shidi instruments, which may compromise the sterility of the product. |
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