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PLS (POSTERIOR LUMBAR SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140787
510(k) Type
Special
Applicant
SINTEA PLUSTEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2014
Days to Decision
60 days
Submission Type
Summary

PLS (POSTERIOR LUMBAR SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140787
510(k) Type
Special
Applicant
SINTEA PLUSTEK, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2014
Days to Decision
60 days
Submission Type
Summary