Last synced on 13 June 2025 at 11:06 pm

ARTFX Lumbar PEEK Cages

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240889
510(k) Type
Traditional
Applicant
ARTFX Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2024
Days to Decision
184 days
Submission Type
Summary

ARTFX Lumbar PEEK Cages

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240889
510(k) Type
Traditional
Applicant
ARTFX Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2024
Days to Decision
184 days
Submission Type
Summary