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FDA 510(k), K133906, C-JAWS CERVICAL COMPRESSIVE STAPLE
FDA 510(k), K133906, C-JAWS CERVICAL COMPRESSIVE STAPLE
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510(K) Number: K133906
Device Name: C-JAWS CERVICAL COMPRESSIVE STAPLE
Manufacturer: MEDICREA INTERNATIONAL
Device Classification Name: anterior staple as supplemental fixation for fusion
Regulation Number: 888.3060
Classification Product Code: PHQ
Date Received: 12/23/2013
Decision Date: 07/24/2014
Regulation Medical Specialty: Orthopedic
Device Name: C-JAWS CERVICAL COMPRESSIVE STAPLE
Manufacturer: MEDICREA INTERNATIONAL
Device Classification Name: anterior staple as supplemental fixation for fusion
Regulation Number: 888.3060
Classification Product Code: PHQ
Date Received: 12/23/2013
Decision Date: 07/24/2014
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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