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

ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP

K Number: K930189 · Decision Aug 6, 1993
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
74
Review Days
204

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Basic Information

Device Name
ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP
K Number
K930189
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Dow Corning Wright
Date Received
January 14, 1993
Decision Date
August 6, 1993
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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Other Clearances by Dow Corning Wright

K Number Device Name
K932210 ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT
K932911 ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT
K934354 LACEY ALL POLYETHYLENE TIBIAL COMPONENT
K932222 SLT FEMORAL HEAD
K932858 ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT
K930228 ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE
K925900 LACEY REVISION FEMORAL COMPONENT
K930188 ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT
K930190 ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP
K926257 ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT
Search all 74 clearances from Dow Corning Wright →