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Results for “nexis®”

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Registry EUDAMED 213 FDA 510(k) incl. De Novo 1 FDA PMA GUDID 180

Country / market European Union (all) 43 United States 181

More countries (1)

France 43

Risk class Class I 65 Class IIa 8 Class IIb 30 Class III Class II (US) 121

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)

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224 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

nexis® SC030024

Novastep,France(FDA applicant)

Withdrawn Registry: GUDID Class:II
nexis® SC030022

Novastep,France(FDA applicant)

Withdrawn Registry: GUDID Class:II
nexis® SC030018

Novastep,France(FDA applicant)

Withdrawn Registry: GUDID Class:II
Nexis® compressive screws

Novastep,France(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 221-224 of 224

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