510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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NQOClass III

Prosthesis, Spinous Process Spacer/Plate

Unknown
FDA source (opens on fda.gov)

NQO is the FDA product code for Prosthesis, Spinous Process Spacer/Plate, a class III device type. FDA's definition for this code reads: "This device is an interspinous spacer or spinous process plate that is implanted between the spinous processes or attached to the spinous process". As of , FDA records hold no 510(k) clearances under this code and 6 recalls.

Classification record

Product code
NQO
Device name
Prosthesis, Spinous Process Spacer/Plate
FDA definition
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
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
6

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 18 companies shown, in name order