Cleared Traditional

K991957 - CICACARE MANAGEMENT FOR SCARS

K991957 is the FDA 510(k) clearance for CICACARE MANAGEMENT FOR SCARS by Smith & Nephew, Inc.. It is a Class 1 General & Plastic Surgery device (product code MDA) cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K991957 · Smith & Nephew, Inc. · General & Plastic Surgery device
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Jul 1999
Decision
40d
Days
Class 1
Risk

K991957 is an FDA 510(k) clearance for the CICACARE MANAGEMENT FOR SCARS. Classified as Elastomer, Silicone, For Scar Management (product code MDA), Class I - General Controls.

Submitted by Smith & Nephew, Inc. (Largo, US). The FDA issued a Cleared decision on July 20, 1999 after a review of 40 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4025 - 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: 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 Smith & Nephew, Inc. devices

Submission Details

510(k) Number K991957 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1999
Decision Date July 20, 1999
Days to Decision 40 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 115d · This submission: 40d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code MDA Elastomer, Silicone, For Scar Management
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4025
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 - MDA Elastomer, Silicone, For Scar Management

All 8
Devices cleared under the same product code (MDA) and FDA review panel - the closest regulatory comparables to K991957.
GELZONE
K013732 · Implantech Associates, Inc. · Feb 2002
CONFORM SHEETING, MODEL IGEL
K012419 · Implantech Associates, Inc. · Oct 2001
CICACARE ROLL-ON GEL-SCAR MANAGEMENT LIQUID GEL.
K991968 · Smith & Nephew, Inc. · Jul 1999
IMPLATECH RP MEDICAL GRADE SILICONE GEL SHEETING
K964846 · Implantech Associates, Inc. · Feb 1997
MENTOR H/S SILICONE GEL SHEETING FOR SCAR MANAGEMENT
K962013 · Mentor Corp. · Aug 1996
CICA-CARE SILICONE GEL SHEET
K935803 · Smith & Nephew United, Inc. · Feb 1994