Atlas FDA

NexGen LPS-Flex/LPS Mobile Bearing Knee System

FDA premarket approval P060037/S073 · decided 2021-12-15

Approval details

PMA number
P060037
Supplement
S073
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
NexGen LPS-Flex/LPS Mobile Bearing Knee System
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Zimmer, Inc.
Date received
2021-06-30
Decision date
2021-12-15
Days to decision
168 days
Decision code
APPR
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Approval to modify the labeling to reflect the findings of the final Post-Approval Study (PAS) report.

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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