Last synced on 25 April 2025 at 11:05 pm

Aries® Lumbar Interbodies

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181347
510(k) Type
Traditional
Applicant
Osseus Fusion Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2018
Days to Decision
86 days
Submission Type
Summary

Aries® Lumbar Interbodies

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181347
510(k) Type
Traditional
Applicant
Osseus Fusion Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2018
Days to Decision
86 days
Submission Type
Summary