ON-X PROSTHETIC HEART VALVE
FDA premarket approval P000037/S004 · decided 2005-05-04
Approval details
- PMA number
- P000037
- Supplement
- S004
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ON-X PROSTHETIC HEART VALVE
- Generic name
- HEART-VALVE, MECHANICAL
- Applicant
- On-X Life Technologies, Inc.
- Date received
- 2005-04-04
- Decision date
- 2005-05-04
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- LWQ
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Kennesaw, GA
- Statement
- CHANGE IN THE MANUFACTURING PROCESS TO INCLUDE AN ADDITIONAL STANDARD LEAFLET INSPECTION STEP FOR REWORKED PRODUCT WITH UNACCEPTABLY HIGH LEAK TEST RESULT.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| CHORD-X PRE-MEASURED LOOPS FOR MITRAL CHORDAL REPLACEMENT (K141060) | On-X Life Technologies, Inc. | 2014-06-06 |