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REMEDY Stemmed Knee Spacer System with All-Poly Tibial Component

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242377
510(k) Type
Traditional
Applicant
OsteoRemedies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2024
Days to Decision
54 days
Submission Type
Summary

REMEDY Stemmed Knee Spacer System with All-Poly Tibial Component

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242377
510(k) Type
Traditional
Applicant
OsteoRemedies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2024
Days to Decision
54 days
Submission Type
Summary