Cleared Traditional

SKIN MESH DEVICE (K861285) - FDA 510(k) Clearance

Class I General & Plastic Surgery device.

K861285 · Precision Modified Devices · General & Plastic Surgery device
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Apr 1986
Decision
10d
Days
Class 1
Risk

K861285 is an FDA 510(k) clearance for the SKIN MESH DEVICE. Classified as Dermatome (product code GFD), Class I - General Controls.

Submitted by Precision Modified Devices (Salt Lake City, US). The FDA issued a Cleared decision on April 17, 1986 after a review of 10 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4820 - 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 Precision Modified Devices devices

Submission Details

510(k) Number K861285 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1986
Decision Date April 17, 1986
Days to Decision 10 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
105d faster than avg
Panel avg: 115d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GFD Dermatome
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4820
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.