Custom Spine, Inc.
Custom Spine, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2015, with 1 FDA device recall on record.
Top product codes for Custom Spine, Inc.
FDA recalls by Custom Spine, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Custom Spine, Inc.
- K143143 — PATHWAY ELIF
- K132596 — PROPOSED OPTIMUS
- K120597 — KOMPREDA
- K111726 — PATHWAY AVID
- K111099 — ISSYS LP SPINAL FIXATION SYSTEM
- K092904 — PATHWAY IVB/VBR
- K091134 — CUSTOM SPINE REGENT ANTERIOR CERVICAL PLATE
- K090566 — PATHWAY AVID
- K080281 — PATHWAY
- K072866 — ISSYS LP SPINAL FIXATION SYSTEM
- K070281 — ISSYS LP SPINAL FIXATION SYSTEM
- K043522 — ISSYS PEDICLE SCREW SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.