Last synced on 25 January 2026 at 3:41 am

STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173347
510(k) Type
Traditional
Applicant
Centinel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
195 days
Submission Type
Summary

STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173347
510(k) Type
Traditional
Applicant
Centinel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2018
Days to Decision
195 days
Submission Type
Summary