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

Inhibitor, Postoperative Fibrosis (Adhesion Barrier)

Unknown
FDA source (opens on fda.gov)

OZJ is the FDA product code for Inhibitor, Postoperative Fibrosis (Adhesion Barrier). FDA's definition for this code reads: "The device is designed to coat surfaces exposed in tendon and peripheral nerve surgery, in order to form a temporary mechanical barrier that separates tissues for the purpose of reducing fibrosis and reducing the formation of adhesions". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
OZJ
Device name
Inhibitor, Postoperative Fibrosis (Adhesion Barrier)
FDA definition
The device is designed to coat surfaces exposed in tendon and peripheral nerve surgery, in order to form a temporary mechanical barrier that separates tissues for the purpose of reducing fibrosis and reducing the formation of adhesions.
Device class
Not classified
Review panel
Unknown
Submission type
Contact ODE
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code