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SYNTEC OSTEO-PLATE AND SCREW FIXATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092889
510(k) Type
Traditional
Applicant
SYNTEC SCIENTIFIC CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
6/25/2010
Days to Decision
277 days
Submission Type
Summary

SYNTEC OSTEO-PLATE AND SCREW FIXATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092889
510(k) Type
Traditional
Applicant
SYNTEC SCIENTIFIC CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
6/25/2010
Days to Decision
277 days
Submission Type
Summary