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NexGen LPS-Flex/LPS Mobile Bearing Knee System

FDA premarket approval P060037/S067 · decided 2020-09-24

Approval details

PMA number
P060037
Supplement
S067
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
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
2020-09-17
Decision date
2020-09-24
Days to decision
7 days
Decision code
OK30
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Replacement of the Prolong UHMWPE crosslinked material specification document, change in references of inspection methodology procedure from the firms internal document to ASTM standards, removal of Free Radical Level by Electron Spin Resonance requirement, and elimination of critical process parameters from the specification document as the ownership of the process is being transferred to a supplier and the supplier will be responsible to maintain these critical process parameters and process m

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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
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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