VERTERA, INC.

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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) (5)

Premarket Exempt

Clear

COALESCE - B14220000132100 Catalog Number :

Device Description : 11x32x10MM COALESCE-Curved, Lordotic

Device Class : 2

Duns Number: 078812764

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

COALESCE - B14220000132110 Catalog Number :

Device Description : 11x32x11MM COALESCE-Curved, Lordotic

Device Class : 2

Duns Number: 078812764

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

COALESCE - B14220000132120 Catalog Number :

Device Description : 11x32x12MM COALESCE-Curved, Lordotic

Device Class : 2

Duns Number: 078812764

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

COALESCE - B14220000132140 Catalog Number :

Device Description : 11x32x14MM COALESCE-Curved, Lordotic

Device Class : 2

Duns Number: 078812764

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

COALESCE - B14220000132160 Catalog Number :

Device Description : 11x32x16MM COALESCE-Curved, Lordotic

Device Class : 2

Duns Number: 078812764

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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