CLARIANCE

Address:18, rue Robespierre,BEAURAINS Hauts-de-France,FR

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Filters

Device Class

Class-1 (A medical device with low to moderate risk that requires general controls) Class-2 (A medical device with a moderate to high risk that requires special controls) Class-3 (A medical device with high risk that requires premarket approval) Class-U (Unclassified)

Product Code

Intervertebral Fusion Device With Bone Graft, Lumbar (MAX) (7) Intervertebral Fusion Device With Bone Graft, Cervical (ODP) (3)

Premarket Exempt

No Yes

Clear

Idys™- LIF - 03700780600403 Catalog Number : 06532908-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600410 Catalog Number : 06532909-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600427 Catalog Number : 06532910-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600434 Catalog Number : 06532911-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600441 Catalog Number : 06532912-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600458 Catalog Number : 06532913-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Idys™- LIF - 03700780600465 Catalog Number : 06532914-S

Device Description : TLIF CAGE

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

KATIA™ - 03700780600557 Catalog Number : 68620035

Device Description : ANTERIOR CERVICAL PLATE 1 LEVEL

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : ODP

Prescription Use : Yes

Device Count : 1

KATIA™ - 03700780600564 Catalog Number : 68620038

Device Description : ANTERIOR CERVICAL PLATE 1 LEVEL

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : ODP

Prescription Use : Yes

Device Count : 1

KATIA™ - 03700780600571 Catalog Number : 68620040

Device Description : ANTERIOR CERVICAL PLATE 1 LEVEL

Device Class : 2

Duns Number: 296568400

Premarket Exempt : No

Product Code : ODP

Prescription Use : Yes

Device Count : 1

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