Last synced on 30 May 2025 at 11:05 pm

LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082679
510(k) Type
Special
Applicant
SINTEA BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
204 days
Submission Type
Summary

LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082679
510(k) Type
Special
Applicant
SINTEA BIOTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2009
Days to Decision
204 days
Submission Type
Summary