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OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131810
510(k) Type
Traditional
Applicant
OSSEUS FUSION SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2013
Days to Decision
50 days
Submission Type
Summary

OSSEUS BLACK DIAMOND PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131810
510(k) Type
Traditional
Applicant
OSSEUS FUSION SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2013
Days to Decision
50 days
Submission Type
Summary