Medtronic Sofamor Danek, Inc.
20 product lines across 1 device categories: Kyphoplasty systems.
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Vertebral Augmentation Systems (Kyphoplasty and Vertebroplasty)
Used in: Kyphoplasty, Vertebroplasty
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| CD HORIZON Fenestrated Screw Set FNS SAS 55751024575 STER CCM 4.5 X 75 | — | 183 | Not stated |
| Medtronic Reusable Instruments TAMP EX1219003 GRAFT | — | 78 | Not stated |
| n/a BONE TAMP KIT KPX103NB AF X2 10/3 | — | 13 | Not stated |
| KYPHON Xpander II KyphoPak Tray BONE TAMP KIT KPX203NB AF X2 20/3 | — | 12 | Not stated |
| KyphPak First Fracture Tray KIT KPX203AB-CDS 20/3 FF ADV WITH CDS | — | 12 | Not stated |
| Medtronic Resuable Instruments PUSHER X0415055 GRAFT | — | 9 | Not stated |
| KyphoPak Tray BONE TAMP KIT KPX153PB FF X2 15/3 1 STP | — | 9 | Not stated |
| KYPHON Xpander II Inflatable Bone Tamp BONE TAMP KX153 15/3 XPANDER II IBT | — | 4 | Not stated |
| KYPHON Express II Inflatable Bone Tamp BONE TAMP KE202 20/2 EXPRESS II IBT | — | 3 | Not stated |
| KYPHON Express Inflatable Bone Tamp BONE TAMP KE152 15/2 EXPRESS II IBT | — | 3 | Not stated |
| ENDOSKELETON TL Graft Tamp, Angled | Length: 12 in | 2 | Not stated |
| KYPHON Xpede Bone Cement BONE CEMENT CX01A XPEDE US | — | 1 | Not stated |
| Kyphon VuE Bone Cement and Kyphon Mixer BONE CEMENT CT01B KYPHON VUE W MIXER | — | 1 | Not stated |
| KYPHON Xpede Bone Cement and KYPHON Mixer Pack BONE CEMENT CX01B XPEDE W MIXER US | — | 1 | Not stated |
| KYPHON HV-R Bone Cement BONE CEMENT C01A HV-R US | — | 1 | Not stated |
| KYPHON HV-R Bone Cement and KYPHON Mixer Pack BONE CEMENT C01B HV-R WITH MIXER US | — | 1 | Not stated |
| KYPHON Inflation Syringe SYRINGE A08E KIS INFLATION HP | — | 1 | Not stated |
| KYPHON ELEMENT INFLATABLE BONE TAMP KR153 15MM VALUEIBT | Outer Diameter: 3 mm; Length: 15 mm | 1 | Not stated |
| ActivOs 10 Bone Cement BONE CEMENT C10A KYPHON ACTIVOS 10 | — | 1 | Not stated |
| ENDOSKELETON TC Tamp | Length: 9 in | 1 | Not stated |
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Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.