FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

MULTIFIT TOTAL HIP SYSTEM

K Number: K101472 · Decision Jan 5, 2011
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
3
Review Days
223

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Basic Information

Device Name
MULTIFIT TOTAL HIP SYSTEM
K Number
K101472
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Otis Biotech Co., Ltd.
Date Received
May 27, 2010
Decision Date
January 5, 2011
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 Otis Biotech Co., Ltd.

K Number Device Name
K170534 PROLIXUS TOTAL KNEE SYSTEM
K083077 ULC SPINAL PEDICLE SCREW SYSTEM