Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Aesculap Implants Systems, LLC

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K231769 activL® Next Generation InstrumentationQLQ2023-07-13 View
510(k) K172235 CoreHip® SystemLZO2018-03-28 View
↑