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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K211663
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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ZAP-X Radiosurgery System, Model: 300150 2 09/26/2025 Zap Surgical Systems
ZAP-X Radiosurgery System 2 09/14/2022 Zap Surgical Systems
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