Last synced on 25 April 2025 at 11:05 pm

SINTEA PLUSTEK 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
K112861
510(k) Type
Special
Applicant
SINTEA PLUSTEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2012
Days to Decision
147 days
Submission Type
Summary

SINTEA PLUSTEK 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
K112861
510(k) Type
Special
Applicant
SINTEA PLUSTEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2012
Days to Decision
147 days
Submission Type
Summary