Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “BICONTACT S/H”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
FDA 510(k) incl. De Novo
FDA PMA
GUDID
Country / market
European Union (all)
United States
More countries (18)
Germany
Italy
Türkiye
France
Netherlands
Spain
Austria
Poland
Belgium
Ireland
Czechia
Portugal
Greece
Sweden
Hungary
Denmark
Romania
Liechtenstein
Risk class
Class I
Class IIa
Class IIb
Class III
Class II (US)
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
2 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Bicontact Hip Stem And Femoral Head
Aesculap
·
,
FDA registration: United States
FDA 510(k)
K040191
Active
Cleared 25 Aug 2004
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Bicontact Hip System With U-Cap
Aesculap
·
,
FDA registration: United States
FDA 510(k)
K043079
Active
Cleared 8 Dec 2004
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Previous
Next
Showing 1-2 of 2