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

Stryker Orthopaedics Hip Systems Labeling Update

K Number: K153345 · Decision May 25, 2016
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
24
Review Days
188

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Basic Information

Device Name
Stryker Orthopaedics Hip Systems Labeling Update
K Number
K153345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Orthopaedics
Date Received
November 19, 2015
Decision Date
May 25, 2016
Product Code
LPH
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
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

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Other Clearances by Stryker Orthopaedics

K Number Device Name
K211703 Insignia Hip Stem
K191414 EXETER Centralizer, EXETER 2.5mm Plug
K173499 Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads
K173849 Triathlon Total Knee System
K172326 Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System
K151264 Restoration Anatomic Shell
K143085 Stryker Orthopaedics Acetabular Shells, Femoral Stems and Total Hip Instruments for use with the Direct Superior Approach
K143393 Triathlon Tritanium Cone Augments
K142462 Restoration Anatomic Shell
K141056 TRIATHLON KNEE SYSTEM POSTERIOR STABILIZED COMPONENTS
Search all 24 clearances from Stryker Orthopaedics →