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KMI CEMENT RESTRICTOR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K061465
510(k) Type
Traditional
Applicant
Kinetikos Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2006
Days to Decision
132 days
Submission Type
Summary

KMI CEMENT RESTRICTOR IMPLANT

Page Type
Cleared 510(K)
510(k) Number
K061465
510(k) Type
Traditional
Applicant
Kinetikos Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
10/5/2006
Days to Decision
132 days
Submission Type
Summary