E-GPS Navigated Instruments
K-Number: K220862 · 2022-07-14
Device Summary
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. The listed applicant is Precision Spine, Inc.. The 510(k) number is K220862.
When did E-GPS Navigated Instruments receive FDA 510(k) clearance?
E-GPS Navigated Instruments received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220862.
Who is the listed applicant for E-GPS Navigated Instruments?
The FDA 510(k) record lists Precision Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E-GPS Navigated Instruments?
The FDA product code for E-GPS Navigated Instruments is OLO.
Other records listing Precision Spine, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OLO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.