FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇿 New Zealand

Enivo™

K Number: K223373 · Decision Apr 7, 2023
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
7
Review Days
154

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Enivo™
K Number
K223373
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aroa Biosurgery , Ltd.
Date Received
November 4, 2022
Decision Date
April 7, 2023
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BTA), ordered by most recent decision date.

View all

Other Clearances by Aroa Biosurgery , Ltd.

K Number Device Name
K250598 Endoform Reconstructive Template - PLGA
K231305 Endoform Dental Membrane
K200502 Myriad Particles
K200413 Symphony
K183398 Endoform Restella
K181935 Endoform Reconstructive Template - Non Absorbable