Cleared Traditional

K922145 - SINOJECT MAXILLARY SINUS PUNCTURE & IRR...

K922145 is an FDA 510(k) clearance for SINOJECT MAXILLARY SINUS PUNCTURE & IRR..., manufactured by Atos Medical AB. The device is a Class 1 General & Plastic Surgery device with product code KAM cleared through the Traditional 510(k) pathway after a 259-day FDA review.

K922145 · Atos Medical AB · General & Plastic Surgery device
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Jan 1993
Decision
259d
Days
Class 1
Risk

K922145 is an FDA 510(k) clearance for the SINOJECT MAXILLARY SINUS PUNCTURE & IRRIGATION SYS. 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 January 21, 1993 after a review of 259 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

FDA 510(k) Submission Details - K922145

510(k) Number K922145 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 1992
Decision Date January 21, 1993
Days to Decision 259 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
144d slower than avg
Panel avg: 115d · This submission: 259d
Pathway characteristics
Predicate-based equivalence.

KAM Device Classification - Class 1, General Controls

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.

Regulatory Peers - KAM Cannula, Sinus

All 16
Devices cleared under the same product code (KAM) and FDA review panel - the closest regulatory comparables to K922145.
ROSSITER SINUS STENT
K951803 · Smith & Nephew Richards, Inc. · May 1995
RAINS FRONTAL SINUS STENT
K951066 · Smith & Nephew Richards, Inc. · Apr 1995
SALMAN SINUS BUTTON
K922902 · Boston Medical Products, Inc. · May 1993
SHIKANI MIDDLE MEATAL ANTROSTOMY VENT TUBE
K912418 · Micromedics, Inc. · Dec 1991
MAXILL-AIR SINUS VENTILATION TUBE
K813474 · Xomed, Inc. · Jan 1982