Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K102248 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Excella II Polyaxial Pedicle Screw used as a pedicle screw system in skeletally mature patients, is ... | 2 | 02/20/2018 |
FEI # 3004719693 Innovasis, Inc |
| Excella II Rod Cat. No.: SR 55100 5.5 x 100 mm LOT 1502 and Excella II Rod Cat. No.: SR 55110 5.5 ... | 2 | 01/19/2016 |
FEI # 3004719693 Innovasis, Inc |
| Excella II Standard Pedicle Screw, Catalog No. E2S47525 and E2S47535, 4.75 mm x 25 mm. For spinal fi... | 2 | 07/16/2014 |
FEI # 3004719693 Innovasis, Inc |
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