Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K220699 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 0081006856766... | 2 | 06/18/2025 | BALT USA, LLC |
| The Prestige Coil System is a product family of embolic coils with associated delivery system compon... | 2 | 02/08/2024 | BALT USA, LLC |
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