Last synced on 25 January 2026 at 3:41 am

STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000333
510(k) Type
Traditional
Applicant
Triad Surgical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
90 days
Submission Type
Statement

STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000333
510(k) Type
Traditional
Applicant
Triad Surgical Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
90 days
Submission Type
Statement