FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

U-MOTION II ACETABULAR SYSTEM

K Number: K122185 · Decision Feb 22, 2013
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
20
Review Days
214

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Basic Information

Device Name
U-MOTION II ACETABULAR SYSTEM
K Number
K122185
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
United Orthopedic Corp.
Date Received
July 23, 2012
Decision Date
February 22, 2013
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 United Orthopedic Corp.

K Number Device Name
K140073 U2 FEMORAL COMPONENT, CR, CEMENTED
K140075 U2 FEMORAL COMPONENT, CR, POROUS COATED
K132455 U-MOTION II PS+ CUP
K122183 AUGMENT AND SCREW, PSA TYPE
K121777 U2 ACETABULAR CUP, PLASMA SPRAY
K111546 U2 HIP SYSTEM
K103497 CERAMIC FEMORAL HEAD
K101670 UNITED U2 BIPOLAR IMPLANT
K100981 UNITED STEM, PSA TYPE
K082424 UNITED U2 TOTAL KNEE SYSTEM
Search all 20 clearances from United Orthopedic Corp. →