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PRIMALOK FACET FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102438
510(k) Type
Traditional
Applicant
Osteomed LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
35 days
Submission Type
Summary

PRIMALOK FACET FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102438
510(k) Type
Traditional
Applicant
Osteomed LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
35 days
Submission Type
Summary