Cleared Traditional

K061700 - NEOTRACT ANCHOR

K061700 is an FDA 510(k) clearance for NEOTRACT ANCHOR, manufactured by Neotract, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GAW cleared through the Traditional 510(k) pathway after a 132-day FDA review.

K061700 · Neotract, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2006
Decision
132d
Days
Class 2
Risk

K061700 is an FDA 510(k) clearance for the NEOTRACT ANCHOR. Classified as Suture, Nonabsorbable, Synthetic, Polypropylene (product code GAW), Class II - Special Controls.

Submitted by Neotract, Inc. (Pleasanton, US). The FDA issued a Cleared decision on October 26, 2006 after a review of 132 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5010 - 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 Neotract, Inc. devices

FDA 510(k) Submission Details - K061700

510(k) Number K061700 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 16, 2006
Decision Date October 26, 2006
Days to Decision 132 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
17d slower than avg
Panel avg: 115d · This submission: 132d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAW Device Classification - Class 2, Special Controls

Product Code GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5010
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GAW Suture, Nonabsorbable, Synthetic, Polypropylene

All 77
Devices cleared under the same product code (GAW) and FDA review panel - the closest regulatory comparables to K061700.
SUTURE PLACEMENT DEVICE AND ACCESSORIES, FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES, LSI R SERIES SUTURE PLACEME
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DIGITEX SUTURE DELIVERY SYSTEM, MODEL 52025, DIGITEX SUTURE CARTRIDGE (SIZE O), MODEL 52026, DIGITEX SUTURE CARTRIDGE
K093112 · Coloplast Manufacturing Us, LLC · Feb 2010
SUTRALENE POLYPROPYLENE SUTURES
K070243 · Visionary Medical Supplies, Inc. · Apr 2007
KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE
K060414 · Kmi Kolster Methods, Inc. · Oct 2006
SUPERSTITCH 5F, 12F, AND EL
K062125 · Sutura, Inc. · Oct 2006
SUPERSTITCH GW, MODELS 06-15-04-GW, 08-15-04-GW
K053482 · Sutura, Inc. · Dec 2005