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

Marker, Suture Identification

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

MAW is the FDA product code for Marker, Suture Identification, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
MAW
Device name
Marker, Suture Identification
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code MAW

By decision year
1 clearance under product code MAW with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MAW by decision year
YearClearances
19891

Applicants with the most clearances

Product code MAW
Applicants holding the most 510(k) clearances under product code MAW
ApplicantClearances
Key Surgical, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MAW.