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SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020085
510(k) Type
Traditional
Applicant
SINTEA BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2002
Days to Decision
334 days
Submission Type
Summary

SINTEA BIOTECH POSTERIOR LUMBAR SYSTEM, MODEL PLS 00.T5.X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020085
510(k) Type
Traditional
Applicant
SINTEA BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2002
Days to Decision
334 days
Submission Type
Summary