510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
MXWClass II

Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride)

21 CFR 878.5010 / General, Plastic Surgery
FDA source (opens on fda.gov)

MXW is the FDA product code for Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride), a class II device type, regulated under 21 CFR 878.5010. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MXW
Device name
Suture, Surgical, Nonabsorbable, Poly (Vinylidene Fluoride)
Regulation
21 CFR 878.5010
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code MXW

By decision year
2 clearances under product code MXW with a decision year between 2006 and 2007, 2006 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MXW by decision year
YearClearances
20061
20071

Applicants with the most clearances

Product code MXW
Applicants holding the most 510(k) clearances under product code MXW
ApplicantClearances
Ethicon, Inc1
Peters Surgical1

Companies listing this code with FDA

Companies whose registered establishments list this code