Atlas FDA

Nexgen LPS-Flex/LPS-Mobile Bearing Knee

FDA premarket approval P060037/S061 · decided 2019-08-07

Approval details

PMA number
P060037
Supplement
S061
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Nexgen LPS-Flex/LPS-Mobile Bearing Knee
Generic name
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing
Applicant
Zimmer, Inc.
Date received
2019-07-11
Decision date
2019-08-07
Days to decision
27 days
Decision code
OK30
Product code
NJL
Advisory committee
Orthopedic
Expedited review
No
Location
Warsaw, IN
Statement
Removal of the cytotoxicity test requirement from the routine process monitoring of the final cleaning process for the NexGen®Complete Knee Solution, Legacy® Knee – Posterior Stabilized (LPS) and the LPS-Flex Mobile Bearing Knee femoral components, at the Shannon, Ireland facility.

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