NFIX II PEDICLE SCREW SYSTEM— 510(k) K061774

Unknown

N Spine, Inc.

FDA 510(k) clearance K061774 for NFIX II PEDICLE SCREW SYSTEM, Unknown on 2006-12-13. Applicant: N Spine, Inc.. Device class: 2.

Clearance details

Applicant: N Spine, Inc.
Product code: Code NQP
Device class: Class 2
Regulation: 21 CFR 888.3070
Advisory panel: Orthopedic
Date received: 2006-06-23
Decision date: 2006-12-13
Decision: Unknown
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.