PMA P030005S137
- Device
- Ingenio™ 2 CRT-P Devices; VALITUDE™ Model: U125; VALITUDE™ X4 Model: U128
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S137
- Product code
- NKE
- Decision date
- 2016-06-20
- Classification
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (crt-p)
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Approval order statement
- Remove the final finish wetblast manufacturing process step.
Current openFDA PMA Record#
- Device
- Ingenio™ 2 CRT-P Devices; VALITUDE™ Model: U125; VALITUDE™ X4 Model: U128
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S137
- Product code
- NKE
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Decision date
- 2016-06-20
- Decision code
- OK30
- Date received
- 2016-05-26
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- Remove the final finish wetblast manufacturing process step.