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TRILOGY AB ACETABULAR SYSTEM

FDA premarket approval P040048/S011 · decided 2010-01-11

Approval details

PMA number
P040048
Supplement
S011
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TRILOGY AB ACETABULAR SYSTEM
Generic name
Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
Applicant
Zimmer, Inc.
Date received
2009-11-23
Decision date
2010-01-11
Days to decision
49 days
Decision code
OK30
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
ADDITION OF AN ALTERNATE TEST METHOD FOR X-RAY DIFFRACTION DETERMINATION (XRD) OF PHASE CONTENT OF THE PLASMA-SPRAYED HYDROXYAPATITE COATINGS AS WELL AS ADDITION OF TWO NEW CONTRACT TESTING FACILITIES (LAMBDA TECHNOLOGIES IN CINCINNATI, OHIO AND EVANS ANALYTICAL GROUP (EAG) IN ROUND ROCK, TEXAS).

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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