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Registry EUDAMED FDA 510(k) incl. De Novo 24 FDA PMA GUDID

Country / market United States 24

Risk class Class I 2 Class IIa Class IIb Class III Class II (US) 22

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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24 devices foundsorted by relevance

Manufacturer: Osteotech, Inc.× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

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Sscs (Segmental Spinal Correction System)

Osteotech, Inc.,United States(FDA applicant) Group of variants

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

Osteotech, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Osteograf 2040 Osteograf 4060

Osteotech, Inc.,United States(FDA applicant)

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

Showing 21-24 of 24

deviCERTS Global Medical Device Regulatory Database

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