STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD— 510(k) K000333

Name: FDA 510(k) clearance K000333
Creator: U.S. Food and Drug Administration
Published: 2000-05-03

Substantially Equivalent

Triad Surgical Technologies, Inc.

FDA 510(k) clearance K000333 for STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD, Substantially Equivalent on 2000-05-03. Applicant: Triad Surgical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Triad Surgical Technologies, Inc.
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2000-02-03
Decision date: 2000-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOS

view all

K161600 — Resection Electrodes2016-09-06
K050923 — LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR2005-05-18
K012684 — REPROCESSED ELECTROSURGICAL ELECTRODE2002-01-18
K011515 — MEDLINE GROUNDING PAD2001-07-13
K003403 — ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 19992001-05-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.