Leksell Gamma Knife C 4 4c

Y/Z-Slides, Standard, SET OF TWO

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
13510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Shaanxi (1), Guangdong (1), Hubei (1).

Chinese manufacturers registered for FDA product code IWB
Manufacturer City Province Registered as Device types
OUR United Corporation Xian Shaanxi Contract manufacturer 2
Masep Medical Science & Technology DEVELOPMENT(SHENZHEN)Co. Shenzhen Guangdong Manufacturer 2
OUR SMD Medical (Wuhan) Co., Ltd. Wuhan Hubei Contract manufacturer 1

Record

Regulatory record for Leksell Gamma Knife C 4 4C
Listed by Elekta Instrument AB, Sweden
FDA product code IWB
Device type System, Radiation Therapy, Radionuclide
Device class Class 2
Regulation 21 CFR 892.5750
Record published 2016-09-24
Record revised 2019-08-12 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Leksell Gamma Knife C 4 4C
Catalogue number Size Per pack Status
1500111 In distribution
1500112 2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GammaPod™ Breast Immobilization and Localization System Xcision Medical Systems, LLC 42
Extend Frame system Elekta Instrument AB 23
Clarity® Elekta Solutions AB 11
Leksell Gamma Knife Icon Elekta Instrument AB 9
Leksell Gamma Knife Perfexion/Icon Elekta Instrument AB 9
Leksell Gamma Knife Perfexion/Icon Elekta Solutions AB 5
Leksell Gamma Knife Icon Elekta Solutions AB 4
GammaBeam Best Theratronics Ltd. 2
Isorad Detector, 15-25MV (-) 3m Sun Nuclear Corporation 2
Leksell GammaPlan Elekta Solutions AB 2
15-25 MV Isorad Detector (3m Cable) Sun Nuclear Corporation 2
Isorad Detector, 6-12MV (+) 3m Sun Nuclear Corporation 2

Showing 12 of 33. All products under System, Radiation Therapy, Radionuclide

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173789 2018-03-30
K173791 2018-02-09
K160440 2016-04-20
K151159 2015-10-29
K151561 2015-08-04
K133565 2014-05-09
K120811 2012-05-24
K092083 2009-09-22
K063512 2007-03-05
K061941 2006-08-21
K061540 2006-07-05
K051022 2005-06-01
K984328 1999-05-21

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2018-06-27 Class II Software design The margin tool in Leksell GammaPlan 11.1 systematically overestimates margin in certain areas of the volume. 52 devices

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer