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OSA RIGID INTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021618
510(k) Type
Traditional
Applicant
OSTEOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2002
Days to Decision
84 days
Submission Type
Summary

OSA RIGID INTERNAL FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021618
510(k) Type
Traditional
Applicant
OSTEOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2002
Days to Decision
84 days
Submission Type
Summary