Cleared Traditional

K091992 - EIDOSMED, MODEL EDG4.0

K091992 is an FDA 510(k) clearance for EIDOSMED, manufactured by Eidosmed, LLC. The device is a Class 2 Orthopedic device with product code OOL cleared through the Traditional 510(k) pathway after a 160-day FDA review.

K091992 · Eidosmed, LLC · Orthopedic device
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Dec 2009
Decision
160d
Days
Class 2
Risk

K091992 is an FDA 510(k) clearance for the EIDOSMED, MODEL EDG4.0. Classified as Electronic Depth Gauge (product code OOL), Class II - Special Controls.

Submitted by Eidosmed, LLC (Deerfield, US). The FDA issued a Cleared decision on December 9, 2009 after a review of 160 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - the FDA orthopedic 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 Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Eidosmed, LLC devices

FDA 510(k) Submission Details - K091992

510(k) Number K091992 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 2009
Decision Date December 09, 2009
Days to Decision 160 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
38d slower than avg
Panel avg: 122d · This submission: 160d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OOL Device Classification - Class 2, Special Controls

Product Code OOL Electronic Depth Gauge
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
Definition For Measuring The Depth Of A Passageway In Bone Or Tissue, Prior To Insertion Of Screws Or Other Hardware. The Device Is An Electronic Depth Gauge For Various Medical Purposes Including, Measuring The Depth Of A Passageway In A Bone Or Other Tissue. It May Enable The Proper Sizing Of Screws And Implants In Medical Procedures.
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 Orthopedic devices follow this clearance model.