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Aesculap Implants Systems, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2023-07-13
TypeNumberDevice NameCodeDateActions
510(k) K231769 activL® Next Generation InstrumentationQLQ2023-07-13 View
510(k) K172235 CoreHip® SystemLZO2018-03-28 View
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