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MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070598
510(k) Type
Traditional
Applicant
Memometal Technologies
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/26/2007
Days to Decision
146 days
Submission Type
Summary

MEMOMETAL INTRA-MEDULLARY BONE FASTENER, MODELS SMART TOE / X-FUSE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070598
510(k) Type
Traditional
Applicant
Memometal Technologies
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/26/2007
Days to Decision
146 days
Submission Type
Summary