Cleared Traditional

K130501 - INTENSIF (FDA 510(k) Clearance)

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K130501 · Endymed Medical, Ltd. · General & Plastic Surgery device
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Mar 2014
Decision
379d
Days
Class 2
Risk

K130501 is an FDA 510(k) clearance for the INTENSIF. Classified as Skin Resurfacing Rf Applicator (product code OUH), Class II - Special Controls.

Submitted by Endymed Medical, Ltd. (Binyamina, IL). The FDA issued a Cleared decision on March 13, 2014 after a review of 379 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Endymed Medical, Ltd. devices

Submission Details

510(k) Number K130501 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 2013
Decision Date March 13, 2014
Days to Decision 379 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
265d slower than avg
Panel avg: 114d · This submission: 379d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code OUH Skin Resurfacing Rf Applicator
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4400
Definition Skin Resurfacing
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.