SpinMedix Absorbable Fibrous Membrane— 510(k) K222220
Substantially EquivalentCelestray Biotech Company, LLC.,
FDA 510(k) clearance K222220 for SpinMedix Absorbable Fibrous Membrane, Substantially Equivalent on 2023-07-06. Applicant: Celestray Biotech Company, LLC.,. Device class: 2.
Clearance details
- Applicant
- Celestray Biotech Company, LLC.,
- Product code
- Code OWW
- Device class
- Class 2
- Regulation
- 21 CFR 878.3300
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bethesda, MD, US
Recent devices under product code OWW
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