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TRILOGY AB ACETABULAR SYSTEM

FDA premarket approval P040048/S002 · decided 2007-06-08

Approval details

PMA number
P040048
Supplement
S002
Supplement type
135 Review Track For 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
2007-01-26
Decision date
2007-06-08
Days to decision
133 days
Decision code
APPR
Product code
MRA
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
APPROVAL FOR THE ADDITION OF THE ZIMMER MANUFACTURING B.V. FACILITY LOCATED IN PONCE, PUERTO RICO AS AN ALTERNATIVE SITE FOR MANUFACTURING THE VERSYS HERITAGE FEMORAL STEMS.

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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