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PRIMAL OK INTERSPINOUS FUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100354
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2010
Days to Decision
186 days
Submission Type
Summary

PRIMAL OK INTERSPINOUS FUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100354
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2010
Days to Decision
186 days
Submission Type
Summary