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

Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant

Unknown
FDA source (opens on fda.gov)

PNW is the FDA product code for Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant, a class III device type. FDA's definition for this code reads: "The device is a metatarsophalangeal joint cartilage replacement device that is implanted in the metatarsal head of the first metatarsophalangeal joint". As of , FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code
PNW
Device name
Prosthesis, Metatarsophalangeal Joint Cartilage Replacement Implant
FDA definition
The device is a metatarsophalangeal joint cartilage replacement device that is implanted in the metatarsal head of the first metatarsophalangeal joint.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
1

Companies listing this code with FDA

Companies whose registered establishments list this code