Cleared Traditional

K060076 - SURGICOUNT SAFETY-SPONGE SYSTEM

K060076 is an FDA 510(k) clearance for SURGICOUNT SAFETY-SPONGE SYSTEM, manufactured by Surgicount Medical. The device is a Class 1 General & Plastic Surgery device with product code LWH cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K060076 · Surgicount Medical · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2006
Decision
63d
Days
Class 1
Risk

K060076 is an FDA 510(k) clearance for the SURGICOUNT SAFETY-SPONGE SYSTEM. Classified as Counter, Sponge, Surgical (product code LWH), Class I - General Controls.

Submitted by Surgicount Medical (Yorba Linda, US). The FDA issued a Cleared decision on March 14, 2006 after a review of 63 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.2740 - 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 Surgicount Medical devices

FDA 510(k) Submission Details - K060076

510(k) Number K060076 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 10, 2006
Decision Date March 14, 2006
Days to Decision 63 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 115d · This submission: 63d
Pathway characteristics
Predicate-based equivalence.

LWH Device Classification - Class 1, General Controls

Product Code LWH Counter, Sponge, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.2740
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 - LWH Counter, Sponge, Surgical

Devices cleared under the same product code (LWH) and FDA review panel - the closest regulatory comparables to K060076.
MEDLINE SURGICAL SPONGE SCANNER
K061316 · Medline Industries, Inc. · Nov 2006
MARKWELL GAUZE SPONGE
K982260 · Markwell Intl., Inc. · Aug 1998
POCKET COUNT OR SAFETCOUNT
K972302 · Sage Products, Inc. · Jul 1997
DEVON SPONGE COUNTER BAGS
K912824 · Devon Industries, Inc. · Aug 1991
SPONGE COUNTER
K790538 · Devon Industries, Inc. · Apr 1979