Cleared Traditional

K980049 - BONETRAP

K980049 is an FDA 510(k) clearance for BONETRAP, manufactured by Bladhs Plast AB. The device is a Class 1 Dental device with product code EIA cleared through the Traditional 510(k) pathway after a 217-day FDA review.

K980049 · Bladhs Plast AB · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1998
Decision
217d
Days
Class 1
Risk

K980049 is an FDA 510(k) clearance for the BONETRAP. Classified as Unit, Operative Dental (product code EIA), Class I - General Controls.

Submitted by Bladhs Plast AB (Pocono Manor, US). The FDA issued a Cleared decision on August 11, 1998 after a review of 217 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6640 - 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 Bladhs Plast AB devices

FDA 510(k) Submission Details - K980049

510(k) Number K980049 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 06, 1998
Decision Date August 11, 1998
Days to Decision 217 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
90d slower than avg
Panel avg: 127d · This submission: 217d
Pathway characteristics
Predicate-based equivalence.

EIA Device Classification - Class 1, General Controls

Product Code EIA Unit, Operative Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6640
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 - EIA Unit, Operative Dental

All 123
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