510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K223301Substantially Equivalent

ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System

Spinecraft LLC, Westmont IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K223301 is the FDA 510(k) clearance record for ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System, a class II device, cleared for Spinecraft, LLC on under FDA product code OLO (Orthopedic Stereotaxic Instrument). FDA's definition for product code OLO reads: "Stereotaxic guidance during orthopedic surgery procedures. Indicated for Orthopedic joint or spine surgery. Neurological stereotaxic instruments are classified under product code HAW". FDA records list 18 510(k) clearances for Spinecraft, LLC, from to . As of , FDA records show no recalls naming K223301.

Clearance record

Decision date
Received
(266 days to decision)
Product code
OLO Orthopedic Stereotaxic Instrument
Regulation
21 CFR 882.4560
Device class
Class II
Review panel
Neurology
Applicant
Spinecraft, LLC 777 Oakmont Ln., Suite 200, Westmont IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OLO

Trailing 12 months
44 clearances under product code OLO in the twelve months to October 2026, February 2026 the highest month at 10.
Show the numbers
Monthly 510(k) clearances under FDA product code OLO, trailing twelve months
MonthClearances
November 20252
December 20254
January 20262
February 202610
March 20267
April 20262
May 20265
June 20265
July 20266
August 20261
September 20260
October 20260