FDA.report

StarBurst

Primary DI
H7877001013171
Brand
StarBurst
Company
NAVILYST MEDICAL, INC.
Model
700-101317
Device description
RITA StarBurst XL Electrosurgical Device
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Related Records

Product Codes

CodeName
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Product Code Classifications

CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions

SubmissionSupplement
K992693000

Premarket Details

SubmissionSupplementDeviceApplicantDecision dateProduct code
K992693000RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90Rita Medical Systems1999-09-10GEI

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
H7877001013171PrimaryHIBCC0
15051684021234SecondaryGS10

GMDN Terms

TermDefinition
Percutaneous electrosurgical probe, tumour-ablation, monopolarA sterile, semi-flexible, hand-held surgical instrument intended to be percutaneously introduced via a dedicated cannula [under computed tomography (CT), magnetic resonance imaging (MRI), or ultrasound (US) guidance] to deliver radio-frequency current in a monopolar configuration from a system generator to coagulate/ablate tissues (excluding the CNS and heart) for the treatment of tumours (e.g., in the liver); in addition to percutaneous access it might also be intended for laparoscopic and/or open surgical use. It includes one or more distal monopolar electrode(s) which may include temperature-sensing elements; the introduction cannula may be included. This is a single-use device.

Device Sizes

TypeValueUnit
Length25Centimeter

Sterilization Methods

Method

Contacts

PhoneEmail
+1(518)795-1676dgreer@angiodynamics.com

Regulatory Flags

DUNS number
809699023
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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