← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

NQO — Prosthesis, Spinous Process Spacer/Plate

This device is an interspinous spacer or spinous process plate that is implanted between the spinous processes or attached to the spinous process.

DEVICE CLASS
Class III
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
OR
✓ Implant— Life-sustaining— GMP-exempt— Third-party review eligible
3
510(K)/PMA CLEARANCES
pma: 3
0
RECALL ENTRIES

Recent clearances

P110008Companion Spine France · pma2026-05-22
P240043Companion Spine France Sas · pma2026-04-01
P140004Boston Scientific Neuromodulation · pma2024-11-07

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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