Cleared Traditional

K872806 - STICK SPONGE, STRUNG TONSIL SPONGE DOUBLE STRUNG

K872806 · American Silk Sutures, Inc. · General & Plastic Surgery device
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Aug 1987
Decision
21d
Days
-
Risk

K872806 is an FDA 510(k) clearance for the STICK SPONGE, STRUNG TONSIL SPONGE DOUBLE STRUNG. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by American Silk Sutures, Inc. (Lynn, US). The FDA issued a Cleared decision on August 4, 1987 after a review of 21 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 American Silk Sutures, Inc. devices

FDA 510(k) Submission Details - K872806

510(k) Number K872806 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 14, 1987
Decision Date August 04, 1987
Days to Decision 21 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
94d faster than avg
Panel avg: 115d · This submission: 21d
Pathway characteristics
Predicate-based equivalence.

EFQ Device Classification - Class 0,

Product Code EFQ Gauze/sponge, Internal
Device Class -

Regulatory Peers - EFQ Gauze/sponge, Internal

All 157
Devices cleared under the same product code (EFQ) and FDA review panel - the closest regulatory comparables to K872806.
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K871438 · Fraass Survival Systems, Inc. · May 1987