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THORACOLUMBAR, LUMBAR AND SACRAL PLATES AND 6.0 AND 7.0 MM BONE SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081380
510(k) Type
Traditional
Applicant
K2M, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2008
Days to Decision
187 days
Submission Type
Summary

THORACOLUMBAR, LUMBAR AND SACRAL PLATES AND 6.0 AND 7.0 MM BONE SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081380
510(k) Type
Traditional
Applicant
K2M, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2008
Days to Decision
187 days
Submission Type
Summary