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MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964350
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1997
Days to Decision
77 days
Submission Type
Summary

MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964350
510(k) Type
Traditional
Applicant
INTERMEDICS ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1997
Days to Decision
77 days
Submission Type
Summary