FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

Leksell Gamma Knife® (Elekta Esprit); Leksell Gamma Knife® (Icon™); Leksell Gamma Knife® (Perfexion™)

K Number: K250391 · Decision Jul 2, 2025
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
47
Applicant Total
14
Review Days
140

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Basic Information

Device Name
Leksell Gamma Knife® (Elekta Esprit); Leksell Gamma Knife® (Icon™); Leksell Gamma Knife® (Perfexion™)
K Number
K250391
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elekta Solutions AB
Date Received
February 12, 2025
Decision Date
July 2, 2025
Product Code
IWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IWB System, Radiation Therapy, Radionuclide

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IWB), ordered by most recent decision date.

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Other Clearances by Elekta Solutions AB

K Number Device Name
K252002 Monaco RTP System (6.3)
K252188 EMLA (Elekta Evo); EMLA (VersaHD); EMLA (Elekta Harmony Pro); EMLA (Elekta Infintiy); EMLA (Elekta Harmony); EMLA (Elekta Synergy)
K251363 ProKnow DS
K232854 Leksell GammaPlan (LGP)
K223229 MOSAIQ® OIS (Oncology Information System)
K223209 Elekta Unity
K223233 Monaco RTP System
K222047 Leksell Gamma Knife Perfexion, Leksell Gamma Knife Icon, Leksell Gamma Knife - Elekta Esprit (New model variant)
K213787 Monaco RTP System
K212218 Advanced Algorithms for Treatment Management Applications (AATMA)
Search all 14 clearances from Elekta Solutions AB →