TITAN SPINE, LLC

Address:6140 W. EXECUTIVE DR,MEQUON,WI,53092,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) (10)

Premarket Exempt

No Yes

Clear

ENDOSKELETON® TT - 00191375002550 Catalog Number : 4110-2509

Device Description : Interbody Fusion Device Parallel Standard 9mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002567 Catalog Number : 4110-2510

Device Description : Interbody Fusion Device Parallel Standard 10mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002574 Catalog Number : 4110-2511

Device Description : Interbody Fusion Device Parallel Standard 11mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002581 Catalog Number : 4110-2512

Device Description : Interbody Fusion Device Parallel Standard 12mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002598 Catalog Number : 4110-2513

Device Description : Interbody Fusion Device Parallel Standard 13mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002604 Catalog Number : 4110-2514

Device Description : Interbody Fusion Device Parallel Standard 14mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002611 Catalog Number : 4110-3007

Device Description : Interbody Fusion Device Parallel Large 7mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002628 Catalog Number : 4110-3008

Device Description : Interbody Fusion Device Parallel Large 8mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002635 Catalog Number : 4110-3009

Device Description : Interbody Fusion Device Parallel Large 9mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

ENDOSKELETON® TT - 00191375002642 Catalog Number : 4110-3010

Device Description : Interbody Fusion Device Parallel Large 10mm

Device Class : 2

Duns Number: 623316978

Premarket Exempt : No

Product Code : MAX

Prescription Use : Yes

Device Count : 1

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