EVERA S DR & VR ICD, EVERA XT DR & VR ICD, MAXIMO II ICD, PROTECTA ICD & XT ICD, SECURA ICD, VIRTUOSO II DR/VR ICD
FDA premarket approval P980016/S525 · decided 2015-02-27
Approval details
- PMA number
- P980016
- Supplement
- S525
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- EVERA S DR & VR ICD, EVERA XT DR & VR ICD, MAXIMO II ICD, PROTECTA ICD & XT ICD, SECURA ICD, VIRTUOSO II DR/VR ICD
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2015-02-02
- Decision date
- 2015-02-27
- Days to decision
- 25 days
- Decision code
- OK30
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- MANUFACTURING PROCESS CHANGES FOR XE161 CRYSTAL COMPONENT USED IN THE DEVICES.
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