KEOS

Address:1824 COLONIAL VILLAGE LN,Lancaster,PA,17601,US

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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)

Premarket Exempt

Clear

Lumbar IBFD - B084KTS22810100 Catalog Number : KTS2-281010

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810110 Catalog Number : KTS2-281011

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810120 Catalog Number : KTS2-281012

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810130 Catalog Number : KTS2-281013

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810140 Catalog Number : KTS2-281014

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810150 Catalog Number : KTS2-281015

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

Lumbar IBFD - B084KTS22810160 Catalog Number : KTS2-281016

Device Class : 2

Duns Number: 080551837

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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