Medical Device Catalogue

882 devices foundsorted by relevance

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Rampart-O 10-10-41-37

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 10-10-76-39

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 49-02-08

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I
Rampart One Lumbar Interbody Fusion System 102-63-06-4

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Versant Rampage 10307530.VER

Fgx International Inc.,FDA registration: United States

None Registry: GUDID Class:I
Rampart T 83-03-01-14

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart O 83-04-07-32

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-2

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-17

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 49-04-04

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I
Rampart One Lumbar Interbody Fusion System 49-02-07

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I
Rampart One Lumbar Interbody Fusion System 102-63-06-24

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-8

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion Device 10-10-77-8

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart-T 83-01-19-15

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart T 83-03-01-16

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart-O 83-05-01-10

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I
Rampart One Lumbar Interbody Fusion Device 10-10-75-3

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart O 83-04-07-26

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart-O 83-05-01-8

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I

Showing 441-460 of 882

Results for “RAMPA”

Category (EMDN)

Rampart-O 10-10-41-37

Rampart One Lumbar Interbody Fusion System 10-10-76-39

Rampart One Lumbar Interbody Fusion System 49-02-08

Rampart One Lumbar Interbody Fusion System 102-63-06-4

Versant Rampage 10307530.VER

Rampart T 83-03-01-14

Rampart O 83-04-07-32

Rampart One Lumbar Interbody Fusion System 102-63-06-2

Rampart One Lumbar Interbody Fusion System 102-63-06-17

Rampart One Lumbar Interbody Fusion System 49-04-04

Rampart One Lumbar Interbody Fusion System 49-02-07

Rampart One Lumbar Interbody Fusion System 102-63-06-24

Rampart One Lumbar Interbody Fusion System 102-63-06-8

Rampart One Lumbar Interbody Fusion Device 10-10-77-8

Rampart-T 83-01-19-15

Rampart T 83-03-01-16

Rampart-O 83-05-01-10

Rampart One Lumbar Interbody Fusion Device 10-10-75-3

Rampart O 83-04-07-26

Rampart-O 83-05-01-8