Cleared Traditional

K992522 - SPECTRUM DESIGNS SPECTRAGEL

K992522 is an FDA 510(k) clearance for SPECTRUM DESIGNS SPECTRAGEL, manufactured by Spectrum Designs, Inc.. The device is a Class 1 General & Plastic Surgery device with product code MDA cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K992522 · Spectrum Designs, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 1999
Decision
90d
Days
Class 1
Risk

K992522 is an FDA 510(k) clearance for the SPECTRUM DESIGNS SPECTRAGEL. Classified as Elastomer, Silicone, For Scar Management (product code MDA), Class I - General Controls.

Submitted by Spectrum Designs, Inc. (Carpineteria, US). The FDA issued a Cleared decision on October 26, 1999 after a review of 90 days - within the typical 510(k) review window.

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: 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.

FDA 510(k) Submission Details - K992522

510(k) Number K992522 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 28, 1999
Decision Date October 26, 1999
Days to Decision 90 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
25d faster than avg
Panel avg: 115d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

MDA Device Classification - Class 1, General Controls

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 78
Devices cleared under the same product code (MDA) and FDA review panel - the closest regulatory comparables to K992522.
KELO-COTE TOPICAL GEL
K002488 · Advanced Bio-Technologies, Inc. · Jan 2001
OLEEVA FOAM
K002109 · Bio Med Sciences, Inc. · Aug 2000
BLAINE SCARCARE PATCH
K001608 · Blaine Labs, Inc. · Jul 2000
SCAREASE SHEETS & SCAREASE GEL
K991970 · Pillar Surgical · Oct 1999
SOOTHE & SMOOTH SCAR CARE - SILICONE SHEETING
K991312 · Library Medical, Inc. · Aug 1999
SKIN 2 FORTE SILICONE SHEETING
K990651 · United Hospital Technologies, Inc. · Aug 1999