Last synced on 25 April 2025 at 11:05 pm

PREVIEW 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
K062371
510(k) Type
Traditional
Applicant
ALPHASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2006
Days to Decision
112 days
Submission Type
Summary

PREVIEW 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
K062371
510(k) Type
Traditional
Applicant
ALPHASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2006
Days to Decision
112 days
Submission Type
Summary