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

Cerclage, Fixation, Metallic

21 CFR 888.3010 / Orthopedic
FDA source (opens on fda.gov)

NDD is the FDA product code for Cerclage, Fixation, Metallic, a class II device type, regulated under 21 CFR 888.3010. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NDD
Device name
Cerclage, Fixation, Metallic
Regulation
21 CFR 888.3010
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
1
Ingested recalls
0

Clearances, product code NDD

By decision year
1 clearance under product code NDD with a decision year between 2001 and 2001, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NDD by decision year
YearClearances
20011

Applicants with the most clearances

Product code NDD
Applicants holding the most 510(k) clearances under product code NDD
ApplicantClearances
Whiteside Biomechanics, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code NDD.