Cleared Traditional

K991215 - SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZ...

K991215 · Symtex Healthcare Corp. · General & Plastic Surgery device
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Jun 1999
Decision
63d
Days
-
Risk

K991215 is an FDA 510(k) clearance for the SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by Symtex Healthcare Corp. (Walnut, US). The FDA issued a Cleared decision on June 11, 1999 after a review of 63 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 Symtex Healthcare Corp. devices

FDA 510(k) Submission Details - K991215

510(k) Number K991215 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 09, 1999
Decision Date June 11, 1999
Days to Decision 63 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 115d · This submission: 63d
Pathway characteristics
Predicate-based equivalence.

EFQ Device Classification - Class 0,

Product Code EFQ Gauze/sponge, Internal
Device Class -

Regulatory Peers - EFQ Gauze/sponge, Internal

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