Atlas FDA

TRIDENT SYSTEM

FDA premarket approval P000013 · decided 2003-02-03

Approval details

PMA number
P000013
Trade name
TRIDENT SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
Howmedica Osteonics Corp.
Date received
2000-03-02
Decision date
2003-02-03
Days to decision
1068 days
Decision code
APPR
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Mahwah, NJ
Statement
APPROVAL FOR THE OSTEONICS ABC SYSTEM AND TRIDENT SYSTEM. THESE DEVICES ARE INDICATED FOR PATIENTS REQUIRING PRIMARY TOTAL HIP ARTHROPLASTY DUE TO PAINFUL DISABLING JOINT DISEASE OF THE HIP RESULTING FROM NON-INFLAMMATORY DEGENERATIVE ARTHRITIS (OSTEOARTHRITIS, AVASCULAR NECROSIS, TRAUMATIC ARTHRITIS, SLIPPED CAPITAL EPIPHYSIS, PELVIC FRACTURE, FEMORAL FRACTURE, FAILED FRACTURE FIXATION, OR DIASTROPHIC VARIANT).

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510(k) clearances by this applicant

RecordFirmDate
Exeter V40 Femoral Stem, Exeter X3 RimFit Cup (K193429)Howmedica Osteonics Corp.2020-08-13
Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite (K200782)Howmedica Osteonics Corp.2020-05-13
REUNION RSA SHOULDER SYSTEM (K130895)Howmedica Osteonics Corp.2013-12-27
ABG III MONOLITHIC HIP STEM (K123604)Howmedica Osteonics Corp.2013-08-16
DISTAL FEMORAL GROWING PROSTHESIS, TIBIAL ROTATING COMPONENTS, BEARING, AXIS, CIRCLIP, WEDGE (K122015)Howmedica Osteonics Corp.2013-02-22
TRIATHLON ALL-POLYETHYLENE CONDYLAR STABILIZING (CS) TIBIAL IMPLANTS TRIATHLON ALL-POLYETHYLENE POSTERIOR STABILIZING (P (K123166)Howmedica Osteonics Corp.2013-02-14
NOVEL FIT AND FILL STEM (K122853)Howmedica Osteonics Corp.2013-02-01
STRYKER CMF MEDPOR CUSTOMIZED IMPLANT (K121315)Howmedica Osteonics Corp.2012-11-01