Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093075 |
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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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CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM REF: PL731SU- Product Usage: Instrument intended for use in ... | 2 | 09/09/2019 | Aesculap Implant Systems LLC |
CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM REF: PL730SU - Product Usage: Instrument intended for use in... | 2 | 09/09/2019 | Aesculap Implant Systems LLC |
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