TRIMED X-FIX— 510(k) K101375

Substantially Equivalent

TriMed, Inc.

FDA 510(k) clearance K101375 for TRIMED X-FIX, Substantially Equivalent on 2010-09-15. Applicant: TriMed, Inc.. Device class: 2.

Clearance details

Applicant: TriMed, Inc.
Product code: Code NDK
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2010-05-17
Decision date: 2010-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Saugus, 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.