Medical Device Catalogue

882 devices foundsorted by relevance

Clear all

Rampart-O 10-10-41-2

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart-T 83-01-04-16

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-18

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 10-10-76-36

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart T 83-03-34-12

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart-T 83-01-06-16

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 49-02-01-1

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart-T 83-01-19-16

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart T 83-03-01-11

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 49-22-04

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:I
Rampart One Lumbar Interbody Fusion System 49-02-01-11

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion Device 10-10-75-8

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart-O 83-02-10-12

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 49-02-01-31

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-20

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart O 83-04-07-11

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart O 83-04-07-22

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart T Lumbar Interbody Fusion Device 10-10-72-4

Spineology Inc.,United States(FDA applicant)

Withdrawn Registry: GUDID Class:II
Rampart One Lumbar Interbody Fusion System 102-63-06-19

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II
Rampart-O 10-10-41-33

Spineology Inc.,United States(FDA applicant)

None Registry: GUDID Class:II

Showing 561-580 of 882

Results for “RAMPA”

Category (EMDN)

Rampart-O 10-10-41-2

Rampart-T 83-01-04-16

Rampart One Lumbar Interbody Fusion System 102-63-06-18

Rampart One Lumbar Interbody Fusion System 10-10-76-36

Rampart T 83-03-34-12

Rampart-T 83-01-06-16

Rampart One Lumbar Interbody Fusion System 49-02-01-1

Rampart-T 83-01-19-16

Rampart T 83-03-01-11

Rampart One Lumbar Interbody Fusion System 49-22-04

Rampart One Lumbar Interbody Fusion System 49-02-01-11

Rampart One Lumbar Interbody Fusion Device 10-10-75-8

Rampart-O 83-02-10-12

Rampart One Lumbar Interbody Fusion System 49-02-01-31

Rampart One Lumbar Interbody Fusion System 102-63-06-20

Rampart O 83-04-07-11

Rampart O 83-04-07-22

Rampart T Lumbar Interbody Fusion Device 10-10-72-4

Rampart One Lumbar Interbody Fusion System 102-63-06-19

Rampart-O 10-10-41-33