K923041 is an FDA 510(k) clearance for the INTESTINAL SPONGES. Classified as Gauze/sponge, Internal (product code EFQ).
Submitted by Surgic Aid, Inc. (Londonderry, US). The FDA issued a Cleared decision on August 10, 1992 after a review of 52 days - a notably fast clearance 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: 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 Surgic Aid, Inc. devices