Cleared Traditional

K896630 - SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM (FDA 510(k) Clearance)

Class I General & Plastic Surgery device.

K896630 · Atos Medical AB · General & Plastic Surgery device
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Jun 1990
Decision
196d
Days
Class 1
Risk

K896630 is an FDA 510(k) clearance for the SINOVENT MAXILLARY SINUS DRAINAGE SYSTEM. Classified as Cannula, Sinus (product code KAM), Class I - General Controls.

Submitted by Atos Medical AB (Potomac, US). The FDA issued a Cleared decision on June 6, 1990 after a review of 196 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery device framework. 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.

View all Atos Medical AB devices

Submission Details

510(k) Number K896630 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 22, 1989
Decision Date June 06, 1990
Days to Decision 196 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
82d slower than avg
Panel avg: 114d · This submission: 196d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KAM Cannula, Sinus
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.