Last synced on 12 October 2025 at 8:21 pm

C3 ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012881
510(k) Type
Traditional
Applicant
SPINE VISION, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2001
Days to Decision
90 days
Submission Type
Summary

C3 ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012881
510(k) Type
Traditional
Applicant
SPINE VISION, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2001
Days to Decision
90 days
Submission Type
Summary