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TITANIUIM BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853869
510(k) Type
Traditional
Applicant
GEORGE TIEMANN & CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1985
Days to Decision
83 days

TITANIUIM BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853869
510(k) Type
Traditional
Applicant
GEORGE TIEMANN & CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1985
Days to Decision
83 days