Cleared Traditional

K830999 - DAP II BIOPSY GUIDE

K830999 is an FDA 510(k) clearance for DAP II BIOPSY GUIDE, manufactured by Rapid Machine & Tool Corp.. The device is a Class 2 Neurology device with product code HAW cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K830999 · Rapid Machine & Tool Corp. · Neurology device
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Jul 1983
Decision
105d
Days
Class 2
Risk

K830999 is an FDA 510(k) clearance for the DAP II BIOPSY GUIDE. Classified as Neurological Stereotaxic Instrument (product code HAW), Class II - Special Controls.

Submitted by Rapid Machine & Tool Corp. (Mchenry, US). The FDA issued a Cleared decision on July 12, 1983 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4560 - the FDA neurology device 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 Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Rapid Machine & Tool Corp. devices

FDA 510(k) Submission Details - K830999

510(k) Number K830999 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 29, 1983
Decision Date July 12, 1983
Days to Decision 105 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 148d · This submission: 105d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HAW Device Classification - Class 2, Special Controls

Product Code HAW Neurological Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
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 Neurology devices follow this clearance model.

Regulatory Peers - HAW Neurological Stereotaxic Instrument

All 356
Devices cleared under the same product code (HAW) and FDA review panel - the closest regulatory comparables to K830999.
TARGET PROGRAM & EPSON HX-20 COMPUTER
K872877 · Walter Lorenz Surgical, Inc. · Feb 1988
KOMAI CT-STEREOTACTIC APPARATUS AND ACCESSORIES
K861629 · Downs Surgical , Ltd. · Aug 1986
DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY
K851973 · Diasonics, Inc. · Jul 1985
PMT VAXIOM STEREOTACTIC SYS #FX001
K831329 · Progress Mankind Technology · Jun 1983
MENISCECTOMY TRAY #9715
K823424 · Concept, Inc. · Mar 1983
LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER
K812744 · Progress Mankind Technology · Dec 1981