LEAD ANCHORING SLEEVE KIT
FDA premarket approval P030036/S059 · decided 2013-06-19
Approval details
- PMA number
- P030036
- Supplement
- S059
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- LEAD ANCHORING SLEEVE KIT
- Generic name
- Permanent defibrillator electrodes
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2013-05-21
- Decision date
- 2013-06-19
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- NVY
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- ALTERNATE SUPPLIERS FOR THE MANUFACTURE OF MULTIPLE SILICONE COMPONENTS.
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