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ANAX™ OCT Spinal System — U&I Corporation (510(k) K183383)

ANAX™ OCT Spinal System — U&I Corporation (510(k) K183383) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: ANAX™ OCT Spinal System; Applicant: U&I Corporation; Clearance track: 510(k).

Device nameANAX™ OCT Spinal System
ApplicantU&I Corporation
Clearance track510(k)
Submission numberK183383
DecisionSubstantially Equivalent
Decision date2018-12-12
Date received2018-12-06
Product codeNKG
Device class2
Medical specialtyOrthopedic
Applicant locationKR
SourceopenFDA device

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