510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
NNVClass I

Vise, Ossicular Finger, Non-Sterile

21 CFR 874.3540 / Ear, Nose, Throat
FDA source (opens on fda.gov)

NNV is the FDA product code for Vise, Ossicular Finger, Non-Sterile, a class I device type, regulated under 21 CFR 874.3540. FDA's definition for this code reads: "Prosthesis modification instrument for ossicular replacement surgery; see product code JYB". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
NNV
Device name
Vise, Ossicular Finger, Non-Sterile
FDA definition
Prosthesis modification instrument for ossicular replacement surgery; see product code JYB.
Regulation
21 CFR 874.3540
Device class
Class I
Review panel
Ear, Nose, Throat
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code