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
NCAClass II

Clip, Implantable, For Coronary Artery Bypass Graft (Cabg)

21 CFR 878.4300 / General, Plastic Surgery
FDA source (opens on fda.gov)

NCA is the FDA product code for Clip, Implantable, For Coronary Artery Bypass Graft (Cabg), a class II device type, regulated under 21 CFR 878.4300. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NCA
Device name
Clip, Implantable, For Coronary Artery Bypass Graft (Cabg)
Regulation
21 CFR 878.4300
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
3
Ingested recalls
0

Clearances, product code NCA

By decision year
3 clearances under product code NCA with a decision year between 2001 and 2002, 2001 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code NCA by decision year
YearClearances
20012
20021

Applicants with the most clearances

Product code NCA
Applicants holding the most 510(k) clearances under product code NCA
ApplicantClearances
Bypass, Ltd.1
Coalescent Surgical1
St. Jude Medical Cardiovascular Group, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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