RAPIDFLAP LS CRANIAL FLAP FIXATION SYSTEM— 510(k) K130309
Substantially EquivalentBiomet Microfixation
FDA 510(k) clearance K130309 for RAPIDFLAP LS CRANIAL FLAP FIXATION SYSTEM, Substantially Equivalent on 2013-06-17. Applicant: Biomet Microfixation. Device class: 2.
Clearance details
- Applicant
- Biomet Microfixation
- 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
- Bartlett, TN, US
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More clearances from Biomet Microfixation
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