Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Biomet Microfixation OmniMax MMF System”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
FDA 510(k) incl. De Novo
3
FDA PMA
GUDID
1
Country / market
United States
4
Risk class
Class I
Class IIa
Class IIb
Class III
Class II (US)
4
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Verified only
Category (EMDN)
Browse by category
Apply filters
4 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Omnimax Mmf System 46-2463
Biomet Microfixation, Inc
·
,
FDA registration: United States
GUDID
on market
None
Registry:
GUDID
Class
Class:
II
OmniMax MMF System
Biomet Microfixation
·
,
FDA registration: United States
Group of variants
FDA 510(k)
K143336
Active
Cleared 1 Apr 2015
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Previous
Next
Showing 1-4 of 4