Cleared Traditional

K093702 - REPROCESSED ULTRASONIC COAGULATING SHEARS

K093702 · Ascent Healthcare Solutions · General & Plastic Surgery device
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Mar 2010
Decision
93d
Days
-
Risk

K093702 is an FDA 510(k) clearance for the REPROCESSED ULTRASONIC COAGULATING SHEARS. Classified as Single-use Reprocessed Ultrasonic Surgical Instruments (product code NLQ).

Submitted by Ascent Healthcare Solutions (Phoenix, US). The FDA issued a Cleared decision on March 4, 2010 after a review of 93 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

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Submission Details

510(k) Number K093702 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 01, 2009
Decision Date March 04, 2010
Days to Decision 93 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 115d · This submission: 93d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code NLQ Single-use Reprocessed Ultrasonic Surgical Instruments
Device Class -
Definition Single-use Reprocessed Versions Of The Ultrasonic Devices Used In Surgical Procedures Either For Fragmentation, Emulsification And Aspiration Of Soft Tissue And Hard Tissue Or For Ligation Of Vessels (under Product Code “lfl”). Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission.. (70 Fr 56911, Available At Https://www.govinfo.gov/content/pkg/fr-2005-09-29/pdf/05-19510.pdf).

Regulatory Peers - NLQ Single-use Reprocessed Ultrasonic Surgical Instruments

All 15
Devices cleared under the same product code (NLQ) and FDA review panel - the closest regulatory comparables to K093702.
Reprocessed Cordless Ultrasonic Dissection Device
K143562 · Sterilmed, Inc. · May 2015
REPROCESSED HARMONIC SHEAR
K132566 · Sterilmed, Inc. · Jun 2014
REPROCESSED HARMONIC SCALPEL
K111794 · Sterilmed, Inc. · Jan 2012
REPROCESSED HARMONIC SCALPEL
K083060 · Sterilmed, Inc. · Jan 2009
REPROCESSED ULTRASONIC SCALPELS
K043358 · Alliance Medical Corp. · Jun 2005
REPROCESSED HARMONIC SCALPELS
K050343 · Sterilmed, Inc. · Apr 2005