Cleared Traditional

K960093 - PROTEC ROLL GAUZE (FDA 510(k) Clearance)

K960093 · Derivadas Degasa S.A. DE C.V. · General & Plastic Surgery device
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Mar 1996
Decision
74d
Days
-
Risk

K960093 is an FDA 510(k) clearance for the PROTEC ROLL GAUZE. Classified as Gauze/sponge, Internal (product code EFQ).

Submitted by Derivadas Degasa S.A. DE C.V. (Palm Harobor, US). The FDA issued a Cleared decision on March 25, 1996 after a review of 74 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 Derivadas Degasa S.A. DE C.V. devices

Submission Details

510(k) Number K960093 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 11, 1996
Decision Date March 25, 1996
Days to Decision 74 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
40d faster than avg
Panel avg: 114d · This submission: 74d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFQ Gauze/sponge, Internal
Device Class -