Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071929 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NDI P7 Position Sensor, Stereotaxic Instrument | 2 | 05/08/2017 |
FEI # 3003714383 Orthosoft, Inc. dba Zimmer CAS |
| Sesamoid Plasty, Stereotaxic Instrument The Sesamoid Plasty workstation is used to run the tracking... | 2 | 06/02/2017 |
FEI # 3003714383 Orthosoft, Inc. dba Zimmer CAS |
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