Precision Spine Navigation Instrumentation

by Precision Spine, Inc.

510(k) K181606

Precision Spine Navigation Instrumentation is a Class II device made by Precision Spine, Inc., cleared under FDA 510(k) K181606 on 27 Sep 2019, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K181606↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK181606	Date27 Sep 2019Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K181606

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K181606
FDA product code: OLO

Device class: Class II
Regulation: 21 CFR Part 882.4560
Advisory committee: Neurology
FDA decision: SESE Substantially Equivalent

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