Class Class II

prodisc® L Instruments (K250554)

K250554 2025-04-25 Traditional
Home/ Devices/ prodisc® L Instruments (K250554)

Description

prodisc® L Instruments by Centinel Spine, LLC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250554
Clearance Date2025-04-25
Clearance TypeTraditional
Product CodeQLQ
Regulation Number888.4515

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote

Predicate lineage for K250554

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. prodisc® L Instruments (K250554) cites 1 predicate device and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K242869prodisc® L InstrumentsCentinel Spine, LLC2024

Trace the full predicate network for K250554

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

Scroll to Top