UNiD Spine Analyzer
K-Number: K170172 · 2017-05-24
ApplicantMedicrea International
Decision Date2017-05-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
UNiD Spine Analyzer is a medical device manufactured by Medicrea International. It received FDA 510(k) clearance on 2017-05-24 under approval number K170172. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the UNiD Spine Analyzer?
UNiD Spine Analyzer is a medical device that received FDA 510(k) clearance on 2017-05-24. It is manufactured by Medicrea International. The 510(k) number is K170172.
When was UNiD Spine Analyzer approved by the FDA?
UNiD Spine Analyzer received FDA 510(k) clearance on 2017-05-24, under approval number K170172.
What company makes UNiD Spine Analyzer?
UNiD Spine Analyzer is manufactured by Medicrea International.
What is the FDA product code for UNiD Spine Analyzer?
The FDA product code for UNiD Spine Analyzer is LLZ.
Other Devices by Medicrea International
Related Devices (Code: LLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.