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SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEM

Page Type
Cleared 510(K)
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)
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