No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 03760154008907 | FIXIT Knotless threaded anchor | EPAV245KNO | Knotless threaded anchor for single interference in rotator cuff repair - Ø 4.5 Knotless threaded anchor for single interference in rotator cuff repair - Ø 4.5 mm, Length 11.25 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
2 | 03760154008921 | FIXIT Knotless threaded anchor | EPAV265KNO | Knotless threaded anchor for single interference in rotator cuff repair - Ø 6.5 Knotless threaded anchor for single interference in rotator cuff repair - Ø 6.5 mm, Length 14 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
3 | 03760154008914 | FIXIT Knotless threaded anchor | EPAV255KNO | Knotless threaded anchor for single interference in rotator cuff repair - Ø 5.5 Knotless threaded anchor for single interference in rotator cuff repair - Ø 5.5 mm, Length 14 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
4 | 03760154008884 | FIXIT Threaded anchor system | EPA0065CLA | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 6.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
5 | 03760154008860 | FIXIT Threaded anchor system | EPA0055CLA | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 5.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
6 | 03760154008846 | FIXIT Threaded anchor system | EPA0047CLA | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 4.7 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | FIXIT |
7 | 03760304680502 | NON STERILE SAMPLE - NOT FOR IMPLANTATION | 292004 | The RIGIDLOOP adjustable juxtacortical fixation device consists of an adjustable The RIGIDLOOP adjustable juxtacortical fixation device consists of an adjustable nonabsorbable braided loop and titanium button, preloaded with traction threads, designed to be used for ACL reconstruction. THE SAMPLE IS NON-STERILE, NOT INTENDED FOR IMPLANTATION. | MBI | Fastener, Fixation, Nondegradable, Soft Tissue | 2 | RIGIDLOOP Multilig Adjustable Cortical Button |
8 | 03760154008976 | Adjustable juxtacortical fixation device for cortical tunnel = Ø 5 to 10 mm | PULXL21202 | The Pullup® adjustable juxtacortical fixation device consists of an adjustable n The Pullup® adjustable juxtacortical fixation device consists of an adjustable nonabsorbable braided loop and titanium button, preloaded with traction threads, designed to be used for ACL reconstruction. The implant is supplied sterile, ready to use. | MBI | Fastener, Fixation, Nondegradable, Soft Tissue | 2 | PULLUP |
9 | 03760154008969 | Adjustable juxtacortical fixation device for cortical tunnel = Ø 4.5 mm | PULLU21201 | The Pullup® adjustable juxtacortical fixation device consists of an adjustable n The Pullup® adjustable juxtacortical fixation device consists of an adjustable nonabsorbable braided loop and titanium button, preloaded with traction threads, designed to be used for ACL reconstruction. The implant is supplied sterile, ready to use. | MBI | Fastener, Fixation, Nondegradable, Soft Tissue | 2 | PULLUP |
10 | 03760154008280 | Suture Anchor Punch Tap | 110026112 | Ø 5.5 mm & Ø 6.5 mm suture anchor punch tap | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
11 | 03760154008273 | Suture Anchor Punch Tap | 110026111 | Ø4.5 mm suture anchor punch tap | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
12 | 03760154008266 | Double loaded BroadBand suture anchor | 110026110 | Threaded anchor system Ø 6.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
13 | 03760154008259 | Double loaded BroadBand suture anchor | 110026109 | Threaded anchor system Ø 5.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
14 | 03760154008242 | Double loaded BroadBand suture anchor | 110026108 | Threaded anchor system Ø 4.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
15 | 03760154008235 | Double loaded MaxBraid suture anchor | 110026107 | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 6.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
16 | 03760154008228 | Double loaded MaxBraid suture anchor | 110026106 | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 5.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
17 | 03760154008211 | Double loaded MaxBraid suture anchor | 110026105 | Threaded anchor system for rotator cuff repair - CLASSIC - Ø 4.5 mm | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
18 | 03760154007245 | Non-sliding BroadBand | 110026115 | Threaded anchor system Ø 6.5 mm with one Blue non-sliding suture and one White/G Threaded anchor system Ø 6.5 mm with one Blue non-sliding suture and one White/Green sliding suture | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
19 | 03760154007238 | Non-sliding BroadBand | 110026114 | Threaded anchor system Ø 5.5 mm with one Blue non-sliding suture and one White/G Threaded anchor system Ø 5.5 mm with one Blue non-sliding suture and one White/Green sliding suture | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
20 | 03760154007221 | Non-sliding BroadBand | 110026113 | Threaded anchor system Ø 4.5 mm with one Blue non-sliding suture and one White/G Threaded anchor system Ø 4.5 mm with one Blue non-sliding suture and one White/Green sliding suture | MAI | Fastener, Fixation, Biodegradable, Soft Tissue | 2 | ComposiTCP™ |
21 | 03760154007924 | Screw for OTIS-C PLUS plate fixation | EVO9066080 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
22 | 03760154005142 | OTIS-C PLUS Plate - Right | EVO9067522 | 316L stainless steel mini-invasive, anatomically shaped plate for HTO. To be use 316L stainless steel mini-invasive, anatomically shaped plate for HTO. To be used with OTIS-C Plus screws. | HRS | Plate, Fixation, Bone | 2 | OTIS-C PLUS |
23 | 03760154005135 | OTIS-C PLUS Plate - Left | EVO9067722 | 316L stainless steel mini-invasive, anatomically shaped plate for HTO. To be use 316L stainless steel mini-invasive, anatomically shaped plate for HTO. To be used with OTIS-C Plus screws. | HRS | Plate, Fixation, Bone | 2 | OTIS-C PLUS |
24 | 03760154004794 | NON STERILE OTIS-C PLUS Plate | EVONS67622 | NON STERILE 316L stainless mini-invasive OTIS-C PLUS plate. | HRS | Plate, Fixation, Bone | 2 | OTIS-C PLUS |
25 | 03760154004770 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66027 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
26 | 03760154004756 | NON STERILE OTIS-C PLUS Left Plate | EVONS67722 | NON STERILE 316L stainless mini-invasive OTIS-C PLUS plate. | HRS | Plate, Fixation, Bone | 2 | OTIS-C PLUS |
27 | 03760154004749 | NON STERILE OTIS-C PLUS Right Plate | EVONS67522 | NON STERILE 316L stainless mini-invasive OTIS-C PLUS plate. | HRS | Plate, Fixation, Bone | 2 | OTIS-C PLUS |
28 | 03760154004732 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66030 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
29 | 03760154004718 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66050 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
30 | 03760154004701 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66036 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
31 | 03760154004695 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66033 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
32 | 03760154004497 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66055 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
33 | 03760154004480 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66065 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
34 | 03760154004459 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66039 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
35 | 03760154004190 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66060 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
36 | 03760154004169 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66042 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
37 | 03760154004152 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66070 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS p NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. https://gudid.fda.gov/gudid/app/admin/udi/recordDetails.xhtml# | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
38 | 03760154004145 | NON STERILE Screw for OTIS-C PLUS plate fixation | EVONS66045 | NON STERILE 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
39 | 03760154001397 | Screw for OTIS-C PLUS plate fixation | EVO9066075 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
40 | 03760154001281 | Screw for OTIS-C PLUS plate fixation | EVO9066070 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
41 | 03760154001274 | Screw for OTIS-C PLUS plate fixation | EVO9066065 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
42 | 03760154001267 | Screw for OTIS-C PLUS plate fixation | EVO9066060 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
43 | 03760154001250 | Screw for OTIS-C PLUS plate fixation | EVO9066055 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
44 | 03760154001243 | Screw for OTIS-C PLUS plate fixation | EVO9066050 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
45 | 03760154001236 | Screw for OTIS-C PLUS plate fixation | EVO9066045 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
46 | 03760154001229 | Screw for OTIS-C PLUS plate fixation | EVO9066042 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
47 | 03760154001212 | Screw for OTIS-C PLUS plate fixation | EVO9066039 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
48 | 03760154001205 | Screw for OTIS-C PLUS plate fixation | EVO9066036 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
49 | 03760154001199 | Screw for OTIS-C PLUS plate fixation | EVO9066033 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
50 | 03760154001182 | Screw for OTIS-C PLUS plate fixation | EVO9066030 | 316L stainless steel screw, for use with mini-invasive OTIS-C PLUS plate. | HWC | Screw, Fixation, Bone | 2 | OTIS-C PLUS |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00887517241566 | 5015010 | AttraX® Putty, 10cc US | AttraX | NUVASIVE, INC. | |
2 | 00887517241559 | 5015006 | AttraX® Putty, 6cc US | AttraX | NUVASIVE, INC. | |
3 | 00887517241542 | 5015005 | AttraX® Putty, 5cc US | AttraX | NUVASIVE, INC. | |
4 | 00887517241535 | 5015002 | AttraX® Putty, 2cc US | AttraX | NUVASIVE, INC. | |
5 | 00887517241528 | 5015001 | AttraX® Putty, 1cc US | AttraX | NUVASIVE, INC. | |
6 | 00887517239372 | 5010205 | FormaGraft® Strips, Small | FormaGraft | NUVASIVE, INC. | |
7 | 00887517239365 | 5010200 | FormaGraft® Strips, Large | FormaGraft | NUVASIVE, INC. | |
8 | 00887517239310 | 5010125 | FormaGraft® XL Blocks, Large | FormaGraft | NUVASIVE, INC. | |
9 | 00887517238450 | 5010085 | FormaGraft® XL Blocks, Small | FormaGraft | NUVASIVE, INC. | |
10 | 00887517238443 | 5010020 | FormaGraft® Granules, 20cc | FormaGraft | NUVASIVE, INC. | |
11 | 00887517238436 | 5010010 | FormaGraft® Granules, 10cc | FormaGraft | NUVASIVE, INC. | |
12 | 00887517238429 | 5010008 | FormaGraft BMA Needle, 8" Packaged | FormaGraft | NUVASIVE, INC. | |
13 | 00887517238412 | 5010005 | FormaGraft® Granules, 5cc | FormaGraft | NUVASIVE, INC. | |
14 | 00887517237392 | 5010001 | FormaGraft BMA Needle, 6-Port (1) | FormaGraft | NUVASIVE, INC. | |
15 | ECURCOM2550 | 25x50x4 mm | 1 x 5.0 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
16 | ECURCOM2525 | 25x25x2 mm | 1 x 2.5 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
17 | ECURCOM2512 | 25x12x4 mm | 1 x 1.2 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
18 | ECURCOM25100 | 25x100x4 mm | 1 x 10.0cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
19 | ECURCOF6565 | 65x65x6 mm | 1 x 25.0 cc | Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
20 | ECURCOF2550 | 25x50x4 mm | 1 x 0.5 cc | Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
21 | ECURCOF25100 | 25x100x4 mm | 1 x 10.0 cc | Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
22 | ECUR449100 | 100x25x4mm | 1 x 10 cc | Device Name: Matriform StripIndication for Use:Matriform® Si Strip is intended t Device Name: Matriform StripIndication for Use:Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process | Matriform SI-Strip | CURASAN AG |
23 | ECUR449050 | 50x25x4 mm | 1 x 5 cc | Device Name: Matriform SI-StripIndication for Use:Matriform® Si Strip is intende Device Name: Matriform SI-StripIndication for Use:Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process | Matriform SI-Strip | CURASAN AG |
24 | ECUR429100 | 25x100x4mm | 1 x 10 cc | Device Name: Matriform StripMofidication: Flexible Foam Indication for Use:Matri Device Name: Matriform StripMofidication: Flexible Foam Indication for Use:Matriform Strip is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Strip resorbs and is replaced with bone during healing process. | Matriform Strip | CURASAN AG |
25 | ECUR429050 | 25x50x4 mm | 1 x 5 cc | Device Name: Matriform StripMofidication: Flexible FoamIndication for Use:Matrif Device Name: Matriform StripMofidication: Flexible FoamIndication for Use:Matriform Strip is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Strip resorbs and is replaced with bone during healing process. | Matriform Strip | CURASAN AG |
26 | ECUR409100 | 25x100x4 mm | 1 x 10 cc | Device Name: Matriform Extra LargeMofidication: Mouldable FoamIndication for Use Device Name: Matriform Extra LargeMofidication: Mouldable FoamIndication for Use:Matriform Extra Large is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Extra Large resorbs and is replaced with bone during healing process. | Matriform Extra Large | CURASAN AG |
27 | ECUR409050 | 25x50x4 mm | 1 x 5 cc | Device Name: Matriform LargeMofidication: Mouldable FoamIndication for Use:Matri Device Name: Matriform LargeMofidication: Mouldable FoamIndication for Use:Matriform Large is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Large resorbs and is replaced with bone during healing process. | Matriform Large | CURASAN AG |
28 | ECUR409025 | 25x25x4 mm | 1 x 2.5 cc | Device Name: Matriform MediumMofidication: Mouldable FoamIndication for Use:Matr Device Name: Matriform MediumMofidication: Mouldable FoamIndication for Use:Matriform Medium is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Medium resorbs and is replaced with bone during healing process. | Matriform Medium | CURASAN AG |
29 | ECUR409012 | 25x12x4 mm | 1 x 1.2 cc | Device Name: Matriform SmalMofidication: Mouldable FoamIndication for Use:Matrif Device Name: Matriform SmalMofidication: Mouldable FoamIndication for Use:Matriform Smal is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Smal resorbs and is replaced with bone during healing process. | Matriform Smal | CURASAN AG |
30 | 00885556237045 | 717816 | 717816 | STRUCSURE CP - 16CC KIT | STRUCSURE | SMITH & NEPHEW, INC. |
31 | 00885556236994 | 717808 | 717808 | STRUCSURE CP - 8CC KIT | STRUCSURE | SMITH & NEPHEW, INC. |
32 | 00885556236949 | 717805 | 717805 | STRUCSURE CP - 5CC KIT | STRUCSURE | SMITH & NEPHEW, INC. |
33 | 00885074478791 | 7600709 | PUTTY 7600709 MSTRGRFT PUTY 9 CC KIT | MASTERGRAFT®Putty | MEDTRONIC SOFAMOR DANEK, INC. | |
34 | 00885074478784 | 7600706 | PUTTY 7600706 MSTRGRFT PUTY 6 CC KIT | MASTERGRAFT®Putty | MEDTRONIC SOFAMOR DANEK, INC. | |
35 | 00885074478760 | 7600703 | PUTTY 7600703 MSTRGRFT PUTY 3 CC KIT | MASTERGRAFT®Putty | MEDTRONIC SOFAMOR DANEK, INC. | |
36 | 00885074478753 | 7600702 | PUTTY 7600702 MSTRGFT PUTY 1.5 CC KT | MASTERGRAFT®Putty | MEDTRONIC SOFAMOR DANEK, INC. | |
37 | 00885074478715 | 7600701 | PUTTY 7600701 MTRGFT PUTY 0.75 CC KT | MASTERGRAFT®Putty | MEDTRONIC SOFAMOR DANEK, INC. | |
38 | 00885074327266 | 7600305 | BIOLOGICS 7600305 MSTRGRFT MATRX 5CC KIT | MASTERGRAFT® MATRIX | MEDTRONIC SOFAMOR DANEK, INC. | |
39 | 00885074012308 | 7600320 | BIOLOGICS 7600320 MSTRGRFT MATRX 20CC KT | MASTERGRAFT® MATRIX | MEDTRONIC SOFAMOR DANEK, INC. | |
40 | 00885074012292 | 7600310 | BIOLOGICS 7600310 MSTRGRFT MATRX 10CC KT | MASTERGRAFT® MATRIX | MEDTRONIC SOFAMOR DANEK, INC. | |
41 | 00880304706408 | 92-2022 | 92-2022 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Paste | BIOMET ORTHOPEDICS, LLC |
42 | 00880304684881 | 92-2007 | 92-2007 | DBM in a Lipid Carrier with Porous Calcium Granules | StaGraft DBM Plus | BIOMET ORTHOPEDICS, LLC |
43 | 00880304686830 | 92-2003 | 92-2003 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Putty | BIOMET ORTHOPEDICS, LLC |
44 | 00880304686816 | 92-2001 | 92-2001 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Putty | BIOMET ORTHOPEDICS, LLC |
45 | 00880304684874 | 92-2005 | 92-2005 | DBM in a Lipid Carrier with Porous Calcium Granules | StaGraft DBM Plus | BIOMET ORTHOPEDICS, LLC |
46 | 00880304684867 | 92-2004 | 92-2004 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Putty | BIOMET ORTHOPEDICS, LLC |
47 | 00880304684850 | 92-2002 | 92-2002 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Putty | BIOMET ORTHOPEDICS, LLC |
48 | 00880304684836 | 92-2000 | 92-2000 | Demineralized Bone Matrix (DBM) in a Lipid Carrier | StaGraft DBM Putty | BIOMET ORTHOPEDICS, LLC |
49 | 00880304683907 | 92-2006 | 92-2006 | DBM in a Lipid Carrier with Porous Calcium Granules | StaGraft DBM Plus | BIOMET ORTHOPEDICS, LLC |
50 | 00868201000188 | 10 cc | Calcium compound bone void filler (10 cc) | Fortera | VIVORTE, INC |