BLUE SKY BIO PLAN, VERSION .38— 510(k) K090607
Substantially EquivalentBlue Sky Bio, LLC
FDA 510(k) clearance K090607 for BLUE SKY BIO PLAN, VERSION .38, Substantially Equivalent on 2009-04-22. Applicant: Blue Sky Bio, LLC. Device class: 2.
Clearance details
- Applicant
- Blue Sky Bio, LLC
- Product code
- Code LLZ
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grayslake, IL, US
Recent devices under product code LLZ
view allMore clearances from Blue Sky Bio, LLC
view all- K232653 — Blue Sky Plan Software, Blue Sky Bio Aligner Z, and Blue Sky Bio Aligner Z FLX
- K221845 — Blue Sky Bio Aligner G & Blue Sky Plan S/W for Blue Sky Bio Aligner G
- K212785 — Blue Sky Bio Multi One Implant System, Blue Sky Bio Long Implant System, Blue Sky Bio PEEK temporary abutments
- K202026 — Blue Sky Bio CAD-CAM Abutments
- K201919 — Blue Sky Bio TAD
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
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.