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

Nail, Fixation, Bone, Metallic

21 CFR 888.3030 / Orthopedic
FDA source (opens on fda.gov)

NDH is the FDA product code for Nail, Fixation, Bone, Metallic, a class II device type, regulated under 21 CFR 888.3030. As of , FDA records hold no 510(k) clearances under this code and 3 recalls.

Classification record

Product code
NDH
Device name
Nail, Fixation, Bone, Metallic
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
3

Companies listing this code with FDA

Companies whose registered establishments list this code