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

U2 HIP STEM, TI POROUS COATED

K Number: K003237 · Decision Jan 10, 2001
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
560
Applicant Total
20
Review Days
85

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Basic Information

Device Name
U2 HIP STEM, TI POROUS COATED
K Number
K003237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3358
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
United Orthopedic Corp.
Date Received
October 17, 2000
Decision Date
January 10, 2001
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LPH), 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
K122185 U-MOTION II ACETABULAR SYSTEM
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
Search all 20 clearances from United Orthopedic Corp. →