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MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090839
510(k) Type
Special
Applicant
SYNTEC SCIENTIFIC CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/24/2009
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO SYNTEC-TAICHUN NON-STERILE BONE PLATE AND SCREW IMPLANTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090839
510(k) Type
Special
Applicant
SYNTEC SCIENTIFIC CORP.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/24/2009
Days to Decision
28 days
Submission Type
Summary