EXCOR Pediatric Ventricular Assist Device
FDA premarket approval P160035/S026 · decided 2022-06-15
Approval details
- PMA number
- P160035
- Supplement
- S026
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- EXCOR Pediatric Ventricular Assist Device
- Generic name
- Ventricular (assist) bypass
- Applicant
- Berlin Heart, Inc.
- Date received
- 2022-05-16
- Decision date
- 2022-06-15
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- DSQ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- The Woodlands, TX
- Statement
- Manufacturing change to the printed circuit board used in the Berlin Heart EXCOR IKUS Driver.
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