510(k) K192435
K192435 is an FDA 510(k) premarket notification submitted by Nu Vasive, Incorporated for the device "NuVasive NuvaLine". The FDA issued a decision of Substantially Equivalent on Sep 26, 2019. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Nu Vasive, Incorporated has 111 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 26, 2019
- Date Received
- Sep 5, 2019
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type
- 510(k)