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

Anchor, Suture, Bone Fixation, Metallic

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

NOV is the FDA product code for Anchor, Suture, Bone Fixation, Metallic, a class II device type, regulated under 21 CFR 888.3030. FDA's definition for this code reads: "This device is indicated for attaching suture into bone for suspension of the nasal valve and for attaching suture into bone at the lower orbital rim". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
NOV
Device name
Anchor, Suture, Bone Fixation, Metallic
FDA definition
This device is indicated for attaching suture into bone for suspension of the nasal valve and for attaching suture into bone at the lower orbital rim.
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
1
Ingested recalls
1

Clearances, product code NOV

By decision year
1 clearance under product code NOV with a decision year between 2003 and 2003, 2003 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NOV by decision year
YearClearances
20031

Applicants with the most clearances

Product code NOV
Applicants holding the most 510(k) clearances under product code NOV
ApplicantClearances
Mitek Worldwide1

Companies listing this code with FDA

Companies whose registered establishments list this code