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OSTEOMED HAND PLATE AND SCREW FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090522
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2009
Days to Decision
126 days
Submission Type
Summary

OSTEOMED HAND PLATE AND SCREW FIXATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090522
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2009
Days to Decision
126 days
Submission Type
Summary