Liberty SI Lateral Implant System
K-Number: K231923 · 2023-12-05
ApplicantSpinal Simplicity, LLC
Decision Date2023-12-05
Product CodeOUR
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Liberty SI Lateral Implant System is a medical device manufactured by Spinal Simplicity, LLC. It received FDA 510(k) clearance on 2023-12-05 under approval number K231923. The device is classified under product code OUR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Liberty SI Lateral Implant System?
Liberty SI Lateral Implant System is a medical device that received FDA 510(k) clearance on 2023-12-05. It is manufactured by Spinal Simplicity, LLC. The 510(k) number is K231923.
When was Liberty SI Lateral Implant System approved by the FDA?
Liberty SI Lateral Implant System received FDA 510(k) clearance on 2023-12-05, under approval number K231923.
What company makes Liberty SI Lateral Implant System?
Liberty SI Lateral Implant System is manufactured by Spinal Simplicity, LLC.
What is the FDA product code for Liberty SI Lateral Implant System?
The FDA product code for Liberty SI Lateral Implant System is OUR.
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Other Devices by Spinal Simplicity, LLC
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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.