Cleared Traditional

K925130 - NESSY SURESTICK(TM)/STANDARD SURESTICK(TM)

K925130 is the FDA 510(k) clearance for NESSY SURESTICK(TM)/STANDARD SURESTICK(TM) by Laserscope. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 156-day FDA review.

K925130 · Laserscope · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1993
Decision
156d
Days
Class 2
Risk

K925130 is an FDA 510(k) clearance for the NESSY SURESTICK(TM)/STANDARD SURESTICK(TM). Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Laserscope (San Jose, US). The FDA issued a Cleared decision on March 18, 1993 after a review of 156 days - an extended review 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: 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.

View all Laserscope devices

Submission Details

510(k) Number K925130 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 1992
Decision Date March 18, 1993
Days to Decision 156 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
41d slower than avg
Panel avg: 115d · This submission: 156d
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 1136
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K925130.
EXCALIBUR ELECTROSURGICAL UNIT
K924960 · Aspen Laboratories, Inc. · Apr 1993
GRASPERS & SCISSORS (MINIMAL ACCESS SURG INSTR)
K924469 · Conmedcorp · Apr 1993
FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER
K924524 · Valleylab, Inc. · Apr 1993
FOOT CONTROL PENCIL
K926306 · Megadyne Medical Products, Inc. · Feb 1993
FORCE GSU HANDSET W/LAPAROSCOPIC ELECTRODE (28CM)
K924918 · Valleylab, Inc. · Jan 1993
SYMBIOSIS SUCTION-IRRIGATOR
K923563 · Symbiosis Corp. · Nov 1992