510(k) K212038
K212038 is an FDA 510(k) premarket notification submitted by K&J Consulting Corporation for the device "K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage". The FDA issued a decision of Substantially Equivalent on August 27, 2021. The device falls under product code ODP (Intervertebral Fusion Device With Bone Graft, Cervical), a Class II device regulated under 21 CFR 888.3080. K&J Consulting Corporation has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 2021
- Date Received
- June 30, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Intervertebral Fusion Device With Bone Graft, Cervical
- Device Class
- Class II
- Regulation Number
- 888.3080
- Review Panel
- OR
- Submission Type
Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.