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STELKAST SURPASS ACETABULAR SYSTEM

FDA premarket approval P040051 · decided 2006-05-12

Approval details

PMA number
P040051
Trade name
STELKAST SURPASS ACETABULAR SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
Stelkast Company
Date received
2004-12-27
Decision date
2006-05-12
Days to decision
501 days
Decision code
APWD
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Mcmurray, PA
Statement
APPROVAL FOR THE STELKAST SURPASS ACETABULAR SYSTEM. THE DEVICE IS INDICATED FOR CEMENTLESS USE IN PRIMARY TOTAL HIP ARTHROPLASTY IN SKELETALLY MATURE INDIVIDUALS WITH NON-INFLAMMATORY DEGENERATIVE JOINT DISEASE SUCH AS OSTEOARTHRITIS, AVASCULAR NECROSIS, CONGENITAL HIP DYSPLASIA, AND TRAUMATIC ARTHRITIS.

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510(k) clearances by this applicant

RecordFirmDate
EXP TIBIAL INSERTS AND PATELLAR COMPONENTS FOR THE PROVEN GEN-FLEX TOTAL KNEE SYSTEM (K122883)Stelkast Company2013-08-05
CROSS-OVER ACETABULAR SHELL & LINER (K122773)Stelkast Company2012-10-09
EXP ACETABULAR LINER, MODELS SC3342 NON-HOODED 28MM, SC3343 HOODED 28MM (K094035)Stelkast Company2011-03-24
PROVEN STEM EXTENDER (K081458)Stelkast Company2008-06-06
PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT (K063211)Stelkast Company2007-01-18
PROVEN REVISION MODULAR TIBIAL TRAY (K051976)Stelkast Company2005-10-17
STELKAST 32MM MODULAR CERAMIC FEMORAL HEAD (K033944)Stelkast Company2004-03-12
STELKAST UNICONDYLAR KNEE SYSTEM (K032824)Stelkast Company2003-11-13