Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K160584 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SNP.... | 2 | 10/24/2025 |
FEI # 3010197287 Surgical Theater Inc |
| Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3.12.0, ima... | 2 | 10/24/2025 |
FEI # 3010197287 Surgical Theater Inc |
| Surgical Navigation Advanced Platform (SNAP), software version SNP.3.12.0, imaging processing radiol... | 2 | 10/24/2025 |
FEI # 3010197287 Surgical Theater Inc |
| Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP), software version SNP.1.12.... | 2 | 10/24/2025 |
FEI # 3010197287 Surgical Theater Inc |
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