Last synced on 6 June 2025 at 11:06 pm

INTAI BONE PLATE AND BONE SCREW SYSTEM; INTAI DHS/DCS PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063020
510(k) Type
Traditional
Applicant
INTAI TECHNOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
73 days
Submission Type
Summary

INTAI BONE PLATE AND BONE SCREW SYSTEM; INTAI DHS/DCS PLATE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063020
510(k) Type
Traditional
Applicant
INTAI TECHNOLOGY INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2006
Days to Decision
73 days
Submission Type
Summary