MACROPORENS CRANILOC— 510(k) K002334
Substantially EquivalentMacropore Biosurgery, Inc.
FDA 510(k) clearance K002334 for MACROPORENS CRANILOC, Substantially Equivalent on 2001-05-02. Applicant: Macropore Biosurgery, Inc.. Device class: 2.
Clearance details
- Applicant
- Macropore Biosurgery, Inc.
- Product code
- Code GXR
- Device class
- Class 2
- Regulation
- 21 CFR 882.5250
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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More clearances from Macropore Biosurgery, Inc.
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