K090767
UnknownPERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
- Applicant
- Interventional Spine, Inc.
- Product code
- MRW
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Special
- Location
- Irvine, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.