Cleared Traditional

K083060 - REPROCESSED HARMONIC SCALPEL

K083060 · Sterilmed, Inc. · General & Plastic Surgery device
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Jan 2009
Decision
87d
Days
-
Risk

K083060 is an FDA 510(k) clearance for the REPROCESSED HARMONIC SCALPEL. Classified as Single-use Reprocessed Ultrasonic Surgical Instruments (product code NLQ).

Submitted by Sterilmed, Inc. (Maple Grove, US). The FDA issued a Cleared decision on January 9, 2009 after a review of 87 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Sterilmed, Inc. devices

FDA 510(k) Submission Details - K083060

510(k) Number K083060 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 14, 2008
Decision Date January 09, 2009
Days to Decision 87 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
28d faster than avg
Panel avg: 115d · This submission: 87d
Pathway characteristics
Predicate-based equivalence.

NLQ Device Classification - Class 0,

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 25
Devices cleared under the same product code (NLQ) and FDA review panel - the closest regulatory comparables to K083060.
REPROCESSED HARMONIC SCALPEL
K111794 · Sterilmed, Inc. · Jan 2012
REPROCESSED ULTRASONIC CURVED SHEARS WITH TORQUE WRENCH AND GRIP ASSIST MODEL FCS9, TWBLUE, GABLUE
K100537 · Ascent Healthcare Solutions · May 2010
REPROCESSED ULTRASONIC COAGULATING SHEARS
K093702 · Ascent Healthcare Solutions · Mar 2010
REPROCESSED ULTRASONIC SCALPELS
K043358 · Alliance Medical Corp. · Jun 2005
REPROCESSED HARMONIC SCALPELS
K050343 · Sterilmed, Inc. · Apr 2005
VANGUARD REPROCESSED ULTRASONIC SCALPEL
K043225 · Vanguard Medical Concepts, Inc. · Mar 2005