Cleared Traditional

K103585 - BOSWORTH AEGIS LINER & RESTORATIVE MATE...

K103585 is the FDA 510(k) clearance for BOSWORTH AEGIS LINER & RESTORATIVE MATE... by Harry J. Bosworth Co.. It is a Class 2 Dental device (product code EMA) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K103585 · Harry J. Bosworth Co. · Dental device
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Mar 2011
Decision
87d
Days
Class 2
Risk

K103585 is an FDA 510(k) clearance for the BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Harry J. Bosworth Co. (Skokie, US). The FDA issued a Cleared decision on March 4, 2011 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - the FDA dental device regulatory 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 Harry J. Bosworth Co. devices

Submission Details

510(k) Number K103585 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 2010
Decision Date March 04, 2011
Days to Decision 87 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 127d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 Dental devices follow this clearance model.

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All 228
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