Atlas FDA

PINNACLE3 RADIATION THERAPY PLANNING SYSTEM

FDA 510(k) clearance K041577 · decided 2004-06-25

Clearance details

K-number
K041577
Device name
PINNACLE3 RADIATION THERAPY PLANNING SYSTEM
Applicant
Adac Laboratories
Decision
Substantially Equivalent
Date received
2004-06-14
Decision date
2004-06-25
Days to decision
11 days
Clearance type
Traditional
Product code
LNH
Device class
2
Regulation number
892.1000
Medical specialty
Radiology
Advisory committee
Radiology
Location
Madison, WI, US
Third-party review
Yes
Expedited review
No

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Recalls involving this device

RecordFirmDate
Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Mode recall (Z-2570-2025)Philips Medical Systems (Cleveland) Inc2025-09-16
Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001 recall (Z-2200-2015)Philips Electronics North America Corporation2015-07-22
Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP sof recall (Z-1643-2015)Philips Medical Systems, Inc.2015-05-21
Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0. recall (Z-1312-2014)Philips Medical Systems (Cleveland), Inc.2014-03-31
Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), Inc., Fitchbu recall (Z-0206-2013)Philips Medical Systems (Cleveland), Inc.2012-11-05
Pinnacle3 Radiation Therapy Planning System, software version 9.0. Model # Description 453 recall (Z-0594-2012)Philips Medical Systems (Cleveland), Inc.2012-01-11
The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; compose recall (Z-1212-2007)Philips Nuclear Medicine, Inc.2007-09-25