Atlas FDA

Aesculap Implant Systems

FDA premarket approval P120024/S005 · decided 2017-04-26

Approval details

PMA number
P120024
Supplement
S005
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
Aesculap Implant Systems
Generic name
Prosthesis, intervertebral disc
Applicant
Highridge Medical, LLC
Date received
2017-02-24
Decision date
2017-04-26
Days to decision
61 days
Decision code
APPR
Product code
MJO
Advisory committee
Orthopedic
Expedited review
No
Location
Westminister, CO
Statement
Approval of changes to the protocol for the post-approval study (PAS) protocol.

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