K231030
- 510(k) number
- K231030
- Device name
- Cove Putty, OsteoCove Putty
- Applicant
- SeaSpine Orthopedics Corporation CA · US
- Product code
- MQV — Filler, Bone Void, Calcium Compound
- Decision date
- 2023-09-14
- Date received
- 2023-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K231030.pdf
Official FDA record: K231030
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.