MAYFIELD Skull Clamp
FDA 510(k) clearance K142238 · decided 2014-11-24
Clearance details
- K-number
- K142238
- Device name
- MAYFIELD Skull Clamp
- Applicant
- Integra LifeSciences Corporation
- Decision
- Substantially Equivalent
- Date received
- 2014-08-13
- Decision date
- 2014-11-24
- Days to decision
- 103 days
- Clearance type
- Traditional
- Product code
- HBL
- Device class
- 2
- Regulation number
- 882.4460
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Planisboro, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.