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PRIMALIF TM LLIF UNITARY PEEK LATERAL LUMBAR INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123207
510(k) Type
Traditional
Applicant
OSTEOMED LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2012
Days to Decision
48 days
Submission Type
Summary

PRIMALIF TM LLIF UNITARY PEEK LATERAL LUMBAR INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123207
510(k) Type
Traditional
Applicant
OSTEOMED LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/29/2012
Days to Decision
48 days
Submission Type
Summary