Corplex P / Theracor P / Allacor P (K231325) - FDA 510(k) Clearance

K231325 is an FDA 510(k) clearance for the Corplex P / Theracor P / Allacor P. Classified as Wound Dressing With Animal-derived Material(s) (product code KGN).

Submitted by Stimlabs, LLC (Roswell, US). The FDA issued a Cleared decision on February 2, 2024 after a review of 270 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.

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