Cervage— 510(k) K172568

Substantially Equivalent

Precifit Medical, Ltd.

FDA 510(k) clearance K172568 for Cervage, Substantially Equivalent on 2018-05-04. Applicant: Precifit Medical, Ltd..

Clearance details

Applicant: Precifit Medical, Ltd.
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2017-08-25
Decision date: 2018-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St Paul, MN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.