Last synced on 25 January 2026 at 3:41 am

Stabilis SA Cervical Stand-Alone System (Various PNs)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251735
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2025
Days to Decision
54 days
Submission Type
Summary

Stabilis SA Cervical Stand-Alone System (Various PNs)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251735
510(k) Type
Traditional
Applicant
Acuity Surgical Devices, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2025
Days to Decision
54 days
Submission Type
Summary