E-GPS Navigated Instruments
K-Number: K220862 · 2022-07-14
ApplicantPrecision Spine, Inc.
Decision Date2022-07-14
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
E-GPS Navigated Instruments is a medical device manufactured by Precision Spine, Inc.. It received FDA 510(k) clearance on 2022-07-14 under approval number K220862. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the E-GPS Navigated Instruments?
E-GPS Navigated Instruments is a medical device that received FDA 510(k) clearance on 2022-07-14. It is manufactured by Precision Spine, Inc.. The 510(k) number is K220862.
When was E-GPS Navigated Instruments approved by the FDA?
E-GPS Navigated Instruments received FDA 510(k) clearance on 2022-07-14, under approval number K220862.
What company makes E-GPS Navigated Instruments?
E-GPS Navigated Instruments is manufactured by Precision Spine, Inc..
What is the FDA product code for E-GPS Navigated Instruments?
The FDA product code for E-GPS Navigated Instruments is OLO.
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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.