Atlas FDA

TRILOGY AB ACETABULAR SYSTEM

FDA premarket approval P040048 · decided 2006-06-28

Approval details

PMA number
P040048
Trade name
TRILOGY AB ACETABULAR SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
Zimmer, Inc.
Date received
2004-12-14
Decision date
2006-06-28
Days to decision
561 days
Decision code
APWD
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR THE TRILOGY AB ACETABULAR SYSTEM. THE DEVICE IS INDICATED FOR EITHER CEMENTED OR NONCEMENTED USE IN SKELETALLY MATURE INDIVIDUALS UNDERGOING PRIMARY SURGERY FOR REHABILITATING HIPS DAMAGED AS A RESULT OF NONINFLAMMATORY DEGENERATIVE JOINT DISEASE (NIDJD) SUCH AS OSTEOARTHRITIS, AVASCULAR NECROSIS, CONGENITAL HIP DYSPLASIA, AND TRAUMATIC ARTHRITIS.

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510(k) clearances by this applicant

RecordFirmDate
Z1 Hip System (K260831)Zimmer, Inc.2026-06-16
Augment Off-Axis Instrument System (K261683)Zimmer, Inc.2026-06-16
Zimmer® Persona® Personalized Knee System (K251840)Zimmer, Inc.2026-05-28
Avenir® Müller Stem; Avenir Complete™ Hip System (K260182)Zimmer, Inc.2026-04-27
Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter) (K253592)Zimmer, Inc.2026-04-13
Affixus Retrograde Femoral Nailing System (K253566)Zimmer, Inc.2026-03-12
Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) (K253189)Zimmer, Inc.2026-03-09
G7® Revision Acetabular System (K252623)Zimmer, Inc.2026-02-04