Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K042125 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of su... | 2 | 06/16/2016 | Musculoskeletal Transplant Foundation, Inc. |
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler) | 2 | 02/09/2024 | Musculoskeletal Transplant Foundation, Inc. |
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler) | 2 | 02/09/2024 | Musculoskeletal Transplant Foundation, Inc. |
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