Precice Max System
K-Number: K232267 · 2023-12-15
Decision Date2023-12-15
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Precice Max System is a medical device manufactured by Nuvasive Specialized Orthopedics, Incorporated. It received FDA 510(k) clearance on 2023-12-15 under approval number K232267. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Precice Max System?
Precice Max System is a medical device that received FDA 510(k) clearance on 2023-12-15. It is manufactured by Nuvasive Specialized Orthopedics, Incorporated. The 510(k) number is K232267.
When was Precice Max System approved by the FDA?
Precice Max System received FDA 510(k) clearance on 2023-12-15, under approval number K232267.
What company makes Precice Max System?
Precice Max System is manufactured by Nuvasive Specialized Orthopedics, Incorporated.
What is the FDA product code for Precice Max System?
The FDA product code for Precice Max System is HSB.
Other Devices by Nuvasive Specialized Orthopedics, Incorporated
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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.