Cleared Traditional

K951714 - CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS S...

K951714 is an FDA 510(k) clearance for CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS S..., manufactured by Cabot Medical Corp.. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K951714 · Cabot Medical Corp. · General & Plastic Surgery device
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Optimized for regulatory review, auditing and printing
Jul 1995
Decision
88d
Days
Class 2
Risk

K951714 is an FDA 510(k) clearance for the CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBER. Classified as Powered Laser Surgical Instrument within the GEX classification (a category for powered laser surgical instruments across multiple specialties), Class II - Special Controls.

Submitted by Cabot Medical Corp. (Langhorne, US). The FDA issued a Cleared decision on July 11, 1995 after a review of 88 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4810 - 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 Cabot Medical Corp. devices

FDA 510(k) Submission Details - K951714

510(k) Number K951714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 14, 1995
Decision Date July 11, 1995
Days to Decision 88 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
27d faster than avg
Panel avg: 115d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEX Device Classification - Class 2, Special Controls

Product Code GEX Powered Laser Surgical Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4810
Definition A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light.
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 - GEX Powered Laser Surgical Instrument

All 1536
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K951714.
SLT MULTIDIMENSIONAL CONTACT LASER SYSTEM
K952813 · Surgical Laser Technologies, Inc. · Jul 1995
CERALAS DIODE LASER SYSTEM (MODEL CERALAS D50)
K951775 · Ceram Optec, Inc. · Jul 1995
MEGABEAM ENDO-ENT PROBE
K952772 · Ceram Optec, Inc. · Jul 1995
MODIFIED COHERENT ULTRAPULSE CO2 SURGICAL LASERS
K951812 · Lumenis, Inc. · Jul 1995
SHARPLAN MODEL 3100 ND:YAG SURGICAL LASER SYSTEM
K951165 · Sharplan Lasers, Inc. · Jun 1995
MEGABEAM ASPIRATING ENDOCULAR PROBE
K952340 · Ceram Optec, Inc. · Jun 1995