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

Tester, Stiffness, Cartilage, Arthroscopic

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

NGR is the FDA product code for Tester, Stiffness, Cartilage, Arthroscopic, a class II 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 no recalls.

Classification record

Product code
NGR
Device name
Tester, Stiffness, Cartilage, Arthroscopic
Regulation
21 CFR 888.1100
Device class
Class II
Review panel
Orthopedic
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code NGR

By decision year
2 clearances under product code NGR with a decision year between 2001 and 2002, 2001 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NGR by decision year
YearClearances
20011
20021

Applicants with the most clearances

Product code NGR
Applicants holding the most 510(k) clearances under product code NGR
ApplicantClearances
Artscan Medical Innovations1
Osteobiologics, 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 NGR.