# K071922: Interplate Interbody Fusion Device, Models C, CGC, L and LGC

- Pathway: 510(k) (Traditional)
- Applicant: Rsb Spine, LLC
- Decided: Sep 18, 2007 after 68 days
- Product code: OVD (Intervertebral Fusion Device With Integrated Fixation, Lumbar)
- Device class: 2
- Regulation: 21 CFR 888.3080
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1,221 later devices descend from it; 5 cite it directly.
1 of 1,222 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K071795: Nuvasive Coroent System (2007), 1,122 descendants of its own
- K082128: Depuy Spine Lateral Cage System (2008), 933 descendants of its own
- K090899: Depuy Spine Lateral System (2009), 932 descendants of its own
- K093242: Patriot Transcontinental Llif Spacer (2009), 921 descendants of its own
- K102293: Caliber Spacer (2011), 869 descendants of its own

## Indications for use
The InterPlate is indicated for anterior screw fixation or intervertebral body fusion of the spine in skeletally mature patients. The device system is designed for use with autograft to facilitate fusion. One device is used per intervertebral space. The InterPlate C and CGC Systems are intended for use at one level in the cervical spine, from C3 to T1, for the treatment of cervical disc disease (defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies). The cervical device is to be used in patients who have had six weeks of non-operative treatment. The InterPlate L and LGC Systems are intended for use at either one level or two contiguous levels in the lumbar spine, from L2 to S1, for the treatment of degenerative disc disease (DDD) with up to Grade | spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The lumbar device is to be used in patients who have had six months of non-operative treatment.

Source page: https://510kreport.com/device/K071922
Methodology: https://510kreport.com/methodology