Cleared Traditional

K980379 - PROWESS PRO-SIM

K980379 is an FDA 510(k) clearance for PROWESS PRO-SIM, manufactured by Ssgi Prowess Systems. The device is a Class 2 Radiology device with product code IYE cleared through the Traditional 510(k) pathway after a 108-day FDA review.

K980379 · Ssgi Prowess Systems · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1998
Decision
108d
Days
Class 2
Risk

K980379 is an FDA 510(k) clearance for the PROWESS PRO-SIM. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Ssgi Prowess Systems (Chico, US). The FDA issued a Cleared decision on May 18, 1998 after a review of 108 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5050 - the FDA radiology and imaging software oversight 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 Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Ssgi Prowess Systems devices

FDA 510(k) Submission Details - K980379

510(k) Number K980379 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 30, 1998
Decision Date May 18, 1998
Days to Decision 108 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
1d slower than avg
Panel avg: 107d · This submission: 108d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYE Device Classification - Class 2, Special Controls

Product Code IYE Accelerator, Linear, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5050
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 Radiology devices follow this clearance model.

Regulatory Peers - IYE Accelerator, Linear, Medical

All 441
Devices cleared under the same product code (IYE) and FDA review panel - the closest regulatory comparables to K980379.
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RADIOCAMERAS PATIENT POSITIONING SYSTEM
K980750 · Surgical Navigation Technologies, Inc. · May 1998
VSS, VIRTUAL SIMULATION SYSTEM
K980629 · Nucletron Corp. · May 1998
CAPINTEC MODEL 292 ELECTROMETER
K980402 · Capintec, Inc. · Apr 1998
CARBON FIBER BREAST BOARD
K974703 · Medtec, Inc. · Mar 1998