FDA 510(k) Applications Submitted by IONICS MEDICAL CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K983667 10/19/1998 IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE IONICS MEDICAL CORP.
K081673 06/13/2008 DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE IONICS MEDICAL CORP.


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