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

ACCOLADE RPS HIP STEM

K Number: K052542 · Decision Sep 27, 2005
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
24
Review Days
12

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Basic Information

Device Name
ACCOLADE RPS HIP STEM
K Number
K052542
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Orthopaedics
Date Received
September 15, 2005
Decision Date
September 27, 2005
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.

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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
K153345 Stryker Orthopaedics Hip Systems Labeling Update
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
Search all 24 clearances from Stryker Orthopaedics →