Cannulated PsiFGuard— 510(k) K241895
Substantially EquivalentSpineguard
FDA 510(k) clearance K241895 for Cannulated PsiFGuard, Substantially Equivalent on 2024-09-26. Applicant: Spineguard. Device class: 2.
Clearance details
- Applicant
- Spineguard
- Product code
- Code SCY
- Device class
- Class 2
- Regulation
- 21 CFR 888.3040
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Vincennes, FR
Data sourced from openFDA. This site is unofficial and independent of the FDA.