Atlas FDA

prodisc L

FDA premarket approval P050010/S022 · decided 2019-12-05

Approval details

PMA number
P050010
Supplement
S022
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
prodisc L
Generic name
Prosthesis, intervertebral disc
Applicant
Centinel Spine, LLC
Date received
2019-09-09
Decision date
2019-12-05
Days to decision
87 days
Decision code
APPR
Product code
MJO
Advisory committee
Orthopedic
Expedited review
No
Location
West Chester, PA
Statement
Approval for modifications to the packaging of the prodisc L

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510(k) clearances by this applicant

RecordFirmDate
prodisc® L Instruments (K250554)Centinel Spine, LLC2025-04-25
prodisc® L Instruments (K242869)Centinel Spine, LLC2024-12-17
prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments (K221848)Centinel Spine, LLC2022-08-19