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

Juveno Hip System Femoral Stem, b-ONE Primary Acetabular System Cups

K Number: K182705 · Decision Feb 14, 2019
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
12
Review Days
140

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Basic Information

Device Name
Juveno Hip System Femoral Stem, b-ONE Primary Acetabular System Cups
K Number
K182705
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
B-One Ortho, Corp.
Date Received
September 27, 2018
Decision Date
February 14, 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

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Other Clearances by B-One Ortho, Corp.

K Number Device Name
K253357 b-ONE® Bipolar Head
K240528 b-ONE® Total Hip System
K222431 b-ONER MOBIO Total Knee System
K213673 b-ONE MOBIO Total Knee System
K212912 OneFix Biocomposite Anchors, OneFix Biocomposite Small Anchors, OneFix All Suture Anchors, OneFix Interference Screws, OneFix Cannula System
K210483 MOBIO Total Knee System
K202768 KOSMO Femoral Stem
K202429 Mobio Total Knee System
K183025 MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component
K180446 b-ONE Total Knee System
Search all 12 clearances from B-One Ortho, Corp. →