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

ARCPM 1050 RESIN-HIPS

K Number: K023357 · Decision Nov 6, 2002
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
34
Review Days
30

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Basic Information

Device Name
ARCPM 1050 RESIN-HIPS
K Number
K023357
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Orthopedics, Inc.
Date Received
October 7, 2002
Decision Date
November 6, 2002
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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K032286 CALCIGEN PSI BONE GRAFT SUBSTITUTE
K030048 HA PMI FEMORAL HIP STEM
K024086 PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM
K023063 COMPREHENSIVE HUMERAL FRACTURE SYSTEM
K023188 PRESS-FIT HEAD RESURFACING DEVICE
K021661 RINGLOC CONSTRAINED LINERS
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