Fusion Robotic Navigation System— 510(k) K232413

Substantially Equivalent

Alphatec Spine, Inc.

FDA 510(k) clearance K232413 for Fusion Robotic Navigation System, Substantially Equivalent on 2023-09-08. Applicant: Alphatec Spine, Inc.. Device class: 2.

Clearance details

Applicant
Alphatec Spine, Inc.
Product code
Code OLO
Device class
Class 2
Regulation
21 CFR 882.4560
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Louisville, CO, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code OLO

view all

More clearances from Alphatec Spine, Inc.

view all

Adverse events under product code OLO

product code OLO
Death
11
Injury
2,799
Malfunction
11,105
Other
1
Total
13,916

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.