SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF— 510(k) K153783

Substantially Equivalent

Spinevision S.A.

FDA 510(k) clearance K153783 for SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF, Substantially Equivalent on 2016-05-04. Applicant: Spinevision S.A..

Clearance details

Applicant: Spinevision S.A.
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2015-12-31
Decision date: 2016-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Antony, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code MAX

product code MAX

Death: 13
Injury: 1,305
Malfunction: 2,885
Total: 4,203

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.