Class Class II
NEXA™ NPWT System (K241515)
Description
NEXA™ NPWT System by Nexa Medical Limited, an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241515
Clearance Date2024-07-26
Clearance TypeTraditional
Product CodeOMP
Regulation Number878.4780
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241515
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. NEXA™ NPWT System (K241515) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162610 | NEXA Negative Pressure Wound Therapy System | Nexa Medical , Ltd. | 2017 |
| K132741 | V.A.C. VIA NEGATIVE PRESSURE WOUND THERAPY SYSTEM | Kci USA, Inc. | 2013 |
Trace the full predicate network for K241515
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.