Atlas FDA

Prestige LP Cervical Disc

FDA premarket approval P090029/S011 · decided 2019-04-26

Approval details

PMA number
P090029
Supplement
S011
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - PAS
Trade name
Prestige LP Cervical Disc
Generic name
Prosthesis, intervertebral disc
Applicant
Medtronic Sofamor Danek USA, Inc.
Date received
2018-10-31
Decision date
2019-04-26
Days to decision
177 days
Decision code
APPR
Product code
MJO
Advisory committee
Orthopedic
Expedited review
No
Location
Memphis, TN
Statement
Approval for labeling updated to include post-approval study results from the continued follow-up of the IDE cohort.

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