IdentiTi ALIF Standalone Interbody System— 510(k) K203742

Substantially Equivalent

Alphatec Spine, Inc.

FDA 510(k) clearance K203742 for IdentiTi ALIF Standalone Interbody System, Substantially Equivalent on 2021-04-09. Applicant: Alphatec Spine, Inc.. Device class: 2.

Clearance details

Applicant
Alphatec Spine, Inc.
Product code
Code OVD
Device class
Class 2
Regulation
21 CFR 888.3080
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Carlsnad, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code OVD

product code OVD
Death
5
Injury
495
Total
500

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.