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

Accessories, Arthroscopic

21 CFR 888.1100 / Orthopedic
FDA source (opens on fda.gov)

NBH is the FDA product code for Accessories, Arthroscopic, a class I device type, regulated under 21 CFR 888.1100. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 55 recalls.

Classification record

Product code
NBH
Device name
Accessories, Arthroscopic
Regulation
21 CFR 888.1100
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
55

Clearances, product code NBH

By decision year
2 clearances under product code NBH with a decision year between 1982 and 1982, 1982 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NBH by decision year
YearClearances
19822

Applicants with the most clearances

Product code NBH
Applicants holding the most 510(k) clearances under product code NBH
ApplicantClearances
Bio-Blitz, Inc.1
Utah Medical Products, Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 259 companies shown, in name order