Cleared Traditional

K151405 - Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology

K151405 · Surgical Instrument Services and Savings(Dba Medline Renewal · General & Plastic Surgery device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jan 2016
Decision
245d
Days
-
Risk

K151405 is an FDA 510(k) clearance for the Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Tec.... Classified as Single-use Reprocessed Ultrasonic Surgical Instruments (product code NLQ).

Submitted by Surgical Instrument Services and Savings(Dba Medline Renewal (Redmond, US). The FDA issued a Cleared decision on January 26, 2016 after a review of 245 days - an extended review 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: 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.

FDA 510(k) Submission Details - K151405

510(k) Number K151405 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 2015
Decision Date January 26, 2016
Days to Decision 245 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
130d slower than avg
Panel avg: 115d · This submission: 245d
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 26
Devices cleared under the same product code (NLQ) and FDA review panel - the closest regulatory comparables to K151405.
Medline ReNewal Reprocessed Sonicision Cordless Ultrasonic Dissector
K170955 · Surgical Instrument Service and Savings Inc.(Dba Medline Ren · Jul 2017
Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology
K170456 · Stryker Sustainability Solutions · Apr 2017
Reprocessed HARMONIC ACE+7, 5 mm Diameter Shears with Advanced Hemostasis
K161693 · Stryker Sustainability Solutions · Feb 2017
Medline ReNewal Reprocessed Harmonic FOCUS+ Shears without Adaptive Tissue Technology
K150524 · Surgical Instrument Services and Savings, Inc. · Dec 2015
Reprocessed Cordless Ultrasonic Dissection Device
K143562 · Sterilmed, Inc. · May 2015
REPROCESSED HARMONIC SHEAR
K132566 · Sterilmed, Inc. · Jun 2014
K151405 · Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology
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