Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K150938 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Straumann Bone Level Implant, ® 4.1mm RC, SLA® 12mm, TiZr, NTP Article Number: 021.4512 | 2 | 08/12/2016 | Straumann Manufacturing, Inc. |
| Straumann Bone Level Implant, ® 4.1mm RC, SLA 10mm, TiZr, NTP Article Number: 021.4510 | 2 | 08/12/2016 | Straumann Manufacturing, Inc. |
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