Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K200030 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten... | 2 | 02/22/2022 | BALT USA, LLC |
| Optima Coil System Model OPTI0520CSF10. For endovascular embolization. | 2 | 09/06/2022 | BALT USA, LLC |
| Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovasc... | 2 | 10/20/2022 | BALT USA, LLC |
| Neurovascular embolization device. The Optima Coil System is a series specialized coils that are ins... | 2 | 02/08/2024 | BALT USA, LLC |
| Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0... | 2 | 06/18/2025 | BALT USA, LLC |
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