Product code IKO
- Device name
- Hammer, Reflex, Powered
- Medical specialty
- Physical Medicine
- Device class
- 2
- Regulation number
- 890.1450
- Review panel
- PM
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset