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Montross Extremity Medical Hemi Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221220
510(k) Type
Traditional
Applicant
Montross Extremity Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
357 days
Submission Type
Summary

Montross Extremity Medical Hemi Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221220
510(k) Type
Traditional
Applicant
Montross Extremity Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2023
Days to Decision
357 days
Submission Type
Summary