Cleared Traditional

Silverlon Wound Contact, Burn Contact Dressings (K190343) - FDA 510(k) Clearance

K190343 · Argentum Medical, LLC · General & Plastic Surgery device
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Optimized for regulatory review, auditing and printing
Jul 2019
Decision
154d
Days
-
Risk

K190343 is an FDA 510(k) clearance for the Silverlon Wound Contact, Burn Contact Dressings. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Argentum Medical, LLC (Geneva, US). The FDA issued a Cleared decision on July 18, 2019 after a review of 154 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 Argentum Medical, LLC devices

Submission Details

510(k) Number K190343 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 2019
Decision Date July 18, 2019
Days to Decision 154 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
PCCP Authorized No
Regulatory Context
Review time vs. panel average
39d slower than avg
Panel avg: 115d · This submission: 154d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

All 168
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