EBI Patient Care, Inc.
2 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a spinal fusion adjunct to recall (Z-2118-2017) | EBI Patient Care, Inc. | 2017-05-26 |
| 10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion adjunct to increa recall (Z-2119-2017) | EBI Patient Care, Inc. | 2017-05-26 |
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Every clearance here is in the API, with alerts when new ones post.