Exactech® Novation® and AcuMatch® E-HXL Acetabular Liners— 510(k) K173583

Substantially Equivalent

Exactech, Inc.

FDA 510(k) clearance K173583 for Exactech® Novation® and AcuMatch® E-HXL Acetabular Liners, Substantially Equivalent on 2018-03-12. Applicant: Exactech, Inc.. Device class: 2.

Clearance details

Applicant
Exactech, Inc.
Product code
Code OQI
Device class
Class 2
Regulation
21 CFR 888.3353
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Gainesville, FL, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K173583

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K173583.

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