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TITANIUM OSSICULAR REPLACMENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030492
510(k) Type
Traditional
Applicant
Invotec International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2003
Days to Decision
12 days
Submission Type
Statement

TITANIUM OSSICULAR REPLACMENT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030492
510(k) Type
Traditional
Applicant
Invotec International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2003
Days to Decision
12 days
Submission Type
Statement