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Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices

FDA product code QLR · Class 2 · Orthopedic

14
Registered devices
0
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Companion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCECompanion Spine DIAM™ Instrumentation — COMPANION SPINE FRANCE

Recent recalls

DateFirmReason
2022-06-14Wright Medical Technology, Inc.The plate cutter is unable to meet sterilization requirements when it is sterilized in a double-wrapped configuration according to the Option 1 Steam Sterilizat

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.