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

POROCOAT POROUS COATING/AML PROXIMALLY-COATED STEM

K Number: K933787 · Decision Apr 13, 1994
Classifications
1
FEI Numbers
271
Registration Numbers
271
Same Product Code
551
Applicant Total
303
Review Days
252

Basic Information

Device Name
POROCOAT POROUS COATING/AML PROXIMALLY-COATED STEM
K Number
K933787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DEPUY, INC.
Date Received
August 4, 1993
Decision Date
April 13, 1994
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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