remede System IPG
FDA premarket approval P160039/S009 · decided 2023-11-09
Approval details
- PMA number
- P160039
- Supplement
- S009
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- remede System IPG
- Generic name
- Implanted phrenic nerve stimulator for central sleep apnea
- Applicant
- Respicardia
- Date received
- 2023-05-01
- Decision date
- 2023-11-09
- Days to decision
- 192 days
- Decision code
- APPR
- Product code
- PSR
- Advisory committee
- Anesthesiology
- Expedited review
- No
- Location
- Minnetonka, MN
- Statement
- approval for introducing ease of use features to aid clinicians when during follow up visits and extending the shelf life the GEN 1.5 Model 1100/1600 IPGs packaging from 2 years to 4 years.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| RESPIGUIDE DELIVERY SYSTEM (K130378) | Respicardia | 2013-10-17 |