Cleared Traditional

K830113 - SEPTOPACK

K830113 is an FDA 510(k) clearance for SEPTOPACK, manufactured by North Pacific Dental, Inc.. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 118-day FDA review.

K830113 · North Pacific Dental, Inc. · Dental device
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May 1983
Decision
118d
Days
Class 2
Risk

K830113 is an FDA 510(k) clearance for the SEPTOPACK. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by North Pacific Dental, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 9, 1983 after a review of 118 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all North Pacific Dental, Inc. devices

FDA 510(k) Submission Details - K830113

510(k) Number K830113 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 11, 1983
Decision Date May 09, 1983
Days to Decision 118 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
10d faster than avg
Panel avg: 128d · This submission: 118d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

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.

Regulatory Peers - EMA Cement, Dental

All 438
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