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SPINEWORKS ANTERIOR LUMBAR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133340
510(k) Type
Traditional
Applicant
SPINEWORKS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2014
Days to Decision
163 days
Submission Type
Summary

SPINEWORKS ANTERIOR LUMBAR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K133340
510(k) Type
Traditional
Applicant
SPINEWORKS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/11/2014
Days to Decision
163 days
Submission Type
Summary