Cleared Traditional

K062337 - MODULAR LAPAROSCOPY ACCESSORIES

Also marketed or referenced as:
SISSORS (STRAIGHT AND CURVED) GRASPER (AGGRESSIVE, ALLIS, ATAUMATIC DISSECTOR

K062337 is the FDA 510(k) clearance for MODULAR LAPAROSCOPY ACCESSORIES by Aaron Medical Industries. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K062337 · Aaron Medical Industries · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2006
Decision
56d
Days
Class 2
Risk

K062337 is an FDA 510(k) clearance for the MODULAR LAPAROSCOPY ACCESSORIES, HANDLE. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Aaron Medical Industries (St. Petersburg, US). The FDA issued a Cleared decision on October 5, 2006 after a review of 56 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4400 - the FDA general and plastic surgery device framework. 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 Aaron Medical Industries devices

Submission Details

510(k) Number K062337 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 10, 2006
Decision Date October 05, 2006
Days to Decision 56 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
59d faster than avg
Panel avg: 115d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GEI Electrosurgical, Cutting & Coagulation & Accessories
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEI Electrosurgical, Cutting & Coagulation & Accessories

All 1137
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K062337.
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K063538 · Arthrocare Corp. · Dec 2006
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K061660 · Stryker Instruments · Oct 2006
ADAPTABLE MONOPOLAR ADAPTABLE AND/OR RETRACTABLE ELECTRODES
K062047 · PAJUNK GmbH Medizintechnologie · Oct 2006
PAJUNKS DISPOSABLE INSERTS FOR HANDLE INSTRUMENTS AND HF ELECTRODES
K062072 · PAJUNK GmbH Medizintechnologie · Sep 2006
STRYKER DISPOSABLE LAPAROSCOPIC SCISSORS
K061225 · Stryker Corp. · Sep 2006
STRYKER SILVERGLIDE BIPOLAR FORCEPS REUSABLE CABLE
K061835 · Stryker Instruments · Sep 2006