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OsteoMed Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K151021
510(k) Type
Special
Applicant
OSTEOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2015
Days to Decision
90 days
Submission Type
Summary

OsteoMed Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K151021
510(k) Type
Special
Applicant
OSTEOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2015
Days to Decision
90 days
Submission Type
Summary