Negative Pressure Wound Therapy Device (V-Move, V-Grand) (K241023)
Description
Negative Pressure Wound Therapy Device (V-Move, V-Grand) by Med Way, Inc., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241023
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Negative Pressure Wound Therapy Device (V-Move, V-Grand) (K241023) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162159 | VCare 1000-300S Pump, VCare 1000-300S System, Perme-foam Dr... | Vr Medical Technologies, LLC | 2017 |
| K132225 | EXTRICARE | Devon Medical, Inc. | 2014 |
Trace the full predicate network for K241023
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.