SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM— 510(k) K132740
Substantially EquivalentSpinefrontier, Inc.
FDA 510(k) clearance K132740 for SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM, Substantially Equivalent on 2013-11-26. Applicant: Spinefrontier, Inc.. Device class: 2.
Clearance details
- Applicant
- Spinefrontier, Inc.
- Product code
- Code NQW
- Device class
- Class 2
- Regulation
- 21 CFR 888.3050
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Beverly, MA, US
Recent devices under product code NQW
view allMore clearances from Spinefrontier, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.