PMA P040003S007
- Device
- EXABLATE 2100 SYSTEM
- Applicant
- Insightec, Ltd.
- PMA number
- P040003
- Supplement
- S007
- Product code
- NRZ
- Decision date
- 2010-04-19
- Classification
- Ablation System, High Intensity Focused Ultrasound (hifu), Mr-guided
- Generic name
- Ablation system, high intensity focused ultrasound (HIFU), MR-guided
- Approval order statement
- APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.
Current openFDA PMA Record#
- Device
- EXABLATE 2100 SYSTEM
- Applicant
- Insightec, Ltd.
- PMA number
- P040003
- Supplement
- S007
- Product code
- NRZ
- Generic name
- Ablation system, high intensity focused ultrasound (HIFU), MR-guided
- Decision date
- 2010-04-19
- Decision code
- APPR
- Date received
- 2010-01-22
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Postapproval Study Protocol - OSB
- Approval order statement
- APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.