Recognized a 510(k)/PMA number — showing its clearance record and devices.
Clearance record K092564
O-ARM IMAGING SYSTEM · Medtronic Navigation, Inc. (Littleton) · decided 2010-06-17 (SESE)
FDA 510(k) database ↗Summary PDF ↗
No GUDID device is registered under this submission yet — registration typically lags clearance by months.
Devices
No matching devices.
Check the spelling, try the All scope, or search by brand, company, UDI barcode, or 3-letter product code.