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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 21 Results
510(K) Number: K062998
 
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Product Description
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FDA Recall
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Compress Device Short Anchor Plug, 10 MM-Correction of revision of unsuccessful osteotomy, arthrodes... 2 11/21/2023 Biomet, Inc.
Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthr... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 12 MM -For Correction of revision of unsuccessful osteotomy, ... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 14 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 18 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 20 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
Compress Device Segmental Anchor Plug, 24 MM-For Correction of revision of unsuccessful osteotomy, a... 2 11/21/2023 Biomet, Inc.
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