INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM— 510(k) K133363

Name: FDA 510(k) clearance K133363
Creator: U.S. Food and Drug Administration
Published: 2014-03-07

Substantially Equivalent

Ldr Spine USA, Inc.

FDA 510(k) clearance K133363 for INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM, Substantially Equivalent on 2014-03-07. Applicant: Ldr Spine USA, Inc.. Device class: 2.

Clearance details

Applicant: Ldr Spine USA, Inc.
Product code: Code PEK
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2013-11-01
Decision date: 2014-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Colorado Springs, CO, 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.