Cleared Traditional

K830925 - MF 380 ELECTROSURGICAL UNIT

K830925 is the FDA 510(k) clearance for MF 380 ELECTROSURGICAL UNIT by Zimmer, Inc.. It is a Class 2 General & Plastic Surgery device (product code GEI) cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K830925 · Zimmer, Inc. · General & Plastic Surgery device
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May 1983
Decision
51d
Days
Class 2
Risk

K830925 is an FDA 510(k) clearance for the MF 380 ELECTROSURGICAL UNIT. Classified as Electrosurgical, Cutting & Coagulation & Accessories within the GEI classification (a category for electrosurgical cutting and coagulation devices), Class II - Special Controls.

Submitted by Zimmer, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 13, 1983 after a review of 51 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 Zimmer, Inc. devices

Submission Details

510(k) Number K830925 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 1983
Decision Date May 13, 1983
Days to Decision 51 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
64d faster than avg
Panel avg: 115d · This submission: 51d
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 1118
Devices cleared under the same product code (GEI) and FDA review panel - the closest regulatory comparables to K830925.
ELECTRODE, FLEXIBLE SUCTION COAGULATOR
K831290 · Aspen Laboratories, Inc. · Jun 1983
160/260 SUCTION COAGULATOR
K830926 · Zimmer, Inc. · Jun 1983
ELECTROSURGICAL UNIT-MF 380 #60-1700
K831291 · Aspen Laboratories, Inc. · Jun 1983
DISPERSIVE ELECTRODE
K830545 · C.R. Bard, Inc. · Mar 1983
MF 360B ELECTROSURGICAL UNIT
K823923 · Aspen Laboratories, Inc. · Feb 1983
3M SCOTCHPLATE 51148 SMALL CONDUCTIVE
K823689 · 3M Company · Jan 1983