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MEMOMETAL INTRA-MEDULLARY BONE FASTENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112197
510(k) Type
Special
Applicant
MEMOMETAL TECHNOLOGIES
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/17/2011
Days to Decision
108 days
Submission Type
Summary

MEMOMETAL INTRA-MEDULLARY BONE FASTENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112197
510(k) Type
Special
Applicant
MEMOMETAL TECHNOLOGIES
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/17/2011
Days to Decision
108 days
Submission Type
Summary