TORQUE INSTRUMENT, MODEL 8500— 510(k) K001476
Substantially EquivalentSpinalight, Inc.
FDA 510(k) clearance K001476 for TORQUE INSTRUMENT, MODEL 8500, Substantially Equivalent on 2000-08-04. Applicant: Spinalight, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Spinalight, Inc.
- Product code
- Code LXM
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kennesaw, GA, US
Recent devices under product code LXM
view allMore clearances from Spinalight, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.