Cleared Traditional

K010277 - AMS FASCIAL-ANCHORING SYSTEM

K010277 is the FDA 510(k) clearance for AMS FASCIAL-ANCHORING SYSTEM by American Medical Systems, Inc.. It is a Class 2 General & Plastic Surgery device (product code NEH) cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K010277 · American Medical Systems, Inc. · General & Plastic Surgery device
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Mar 2001
Decision
55d
Days
Class 2
Risk

K010277 is an FDA 510(k) clearance for the AMS FASCIAL-ANCHORING SYSTEM. Classified as Anchor, Fascial (product code NEH), Class II - Special Controls.

Submitted by American Medical Systems, Inc. (Minnetonka, US). The FDA issued a Cleared decision on March 26, 2001 after a review of 55 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4300 - 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 American Medical Systems, Inc. devices

Submission Details

510(k) Number K010277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 2001
Decision Date March 26, 2001
Days to Decision 55 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
60d faster than avg
Panel avg: 115d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code NEH Anchor, Fascial
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4300
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.