Cleared Traditional

K892904 - MITEK DRILL GUIDE

K892904 is an FDA 510(k) clearance for MITEK DRILL GUIDE, manufactured by Mitek Surgical Products, Inc.. The device is a Class 1 Orthopedic device with product code HXY cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K892904 · Mitek Surgical Products, Inc. · Orthopedic device
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Sep 1989
Decision
161d
Days
Class 1
Risk

K892904 is an FDA 510(k) clearance for the MITEK DRILL GUIDE. Classified as Brace, Drill (product code HXY), Class I - General Controls.

Submitted by Mitek Surgical Products, Inc. (Dedham, US). The FDA issued a Cleared decision on September 28, 1989 after a review of 161 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.4540 - 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 Mitek Surgical Products, Inc. devices

FDA 510(k) Submission Details - K892904

510(k) Number K892904 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 20, 1989
Decision Date September 28, 1989
Days to Decision 161 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
39d slower than avg
Panel avg: 122d · This submission: 161d
Pathway characteristics
Predicate-based equivalence.

HXY Device Classification - Class 1, General Controls

Product Code HXY Brace, Drill
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.4540
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.