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

ZICONIA CERAMIC MOD HEAD(TYPE I TAPER 28/32, +6MM)

K Number: K925345 · Decision Mar 10, 1994
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
441
Review Days
504

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Basic Information

Device Name
ZICONIA CERAMIC MOD HEAD(TYPE I TAPER 28/32, +6MM)
K Number
K925345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Biomet, Inc.
Date Received
October 22, 1992
Decision Date
March 10, 1994
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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