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PATHWAY AVID — Custom Spine, Inc. (510(k) K090566)

PATHWAY AVID — Custom Spine, Inc. (510(k) K090566) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PATHWAY AVID; Applicant: Custom Spine, Inc.; Clearance track: 510(k).

Device namePATHWAY AVID
ApplicantCustom Spine, Inc.
Clearance track510(k)
Submission numberK090566
DecisionSubstantially Equivalent
Decision date2009-06-01
Date received2009-03-03
Product codeMAX
Device class2
Medical specialtyOrthopedic
Applicant locationNJ, US
SourceopenFDA device

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