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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K974025
 
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8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Large Craniotome Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
19cm Attachment, Black Max Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
19CM ATTACHMENT, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
11.25CM ATTACHMENT, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
STANDARD CRANIOTOME, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
KEYLESS DRIVER, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
26.65CM ATTACHMENT, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
12.6CM TAPERED ATTACHMENT, BLACK MAX Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
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