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.
Clearance details
- Applicant
- Biomet Microfixation
- Product code
- Code GXR
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bartlett, TN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.