Spinal Deformity Clinical Trial
Official title:
The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And Core spiNe produCt collEction
The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s). Subjects are enrolled and followed postoperatively for up to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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| Completed |
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| Completed |
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N/A | |
| Active, not recruiting |
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| Completed |
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| Completed |
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| Completed |
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| Active, not recruiting |
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Clinical Safety and Efficacy of S53P4 Bioactive Glass Putty in Spinal Fusion Surgery
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| Completed |
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N/A | |
| Active, not recruiting |
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| Completed |
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N/A | |
| Recruiting |
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| Active, not recruiting |
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N/A | |
| Recruiting |
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| Completed |
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