Redi-Spine— 510(k) K181584
Substantially EquivalentInnovative Surgical Designs, Inc.
FDA 510(k) clearance K181584 for Redi-Spine, Substantially Equivalent on 2018-08-10. Applicant: Innovative Surgical Designs, Inc..
Clearance details
- Applicant
- Innovative Surgical Designs, Inc.
- Product code
- Code NKB
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bloomington, IN, US
Adverse events under product code NKB
product code NKB- Death
- 27
- Injury
- 5,033
- Malfunction
- 4,140
- Total
- 9,200
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.