FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Libertas Acetabular Hooded Liner

K Number: K183365 · Decision Feb 22, 2019
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
23
Review Days
80

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Libertas Acetabular Hooded Liner
K Number
K183365
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Maxx Orthopedics, Inc.
Date Received
December 4, 2018
Decision Date
February 22, 2019
Product Code
LZO
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LZO), ordered by most recent decision date.

View all

Other Clearances by Maxx Orthopedics, Inc.

K Number Device Name
K253171 Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)
K252777 Freedom Metaphyseal Cone Implants (Metaphyseal Cones)
K253314 Freedom Infinia™ Total Knee System
K253144 Freedom® Total Knee System – Titan PCK Components
K243634 Maxx Libertas Bipolar Hip Head (Bipolar Hip)
K251717 Freedom® Total Knee System – Titanium Tibial Base Plate
K250382 Freedom Total Knee System (All-poly Tibial Plate)
K241597 Freedom® Total Knee System - Porous Tibial Base Plate
K243277 Freedom® Medial Congruent Liner
K240863 Freedom® Total Knee System
Search all 23 clearances from Maxx Orthopedics, Inc. →