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SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093820
510(k) Type
Traditional
Applicant
MEMOMETAL TECHNOLOGIES
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/19/2010
Days to Decision
156 days
Submission Type
Summary

SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093820
510(k) Type
Traditional
Applicant
MEMOMETAL TECHNOLOGIES
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/19/2010
Days to Decision
156 days
Submission Type
Summary