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FDA 510(k)

C-JAWS CERVICAL COMPRESSIVE MINI FRAME

K-Number: K062181 · 2007-01-16

ApplicantMedicrea Technologies
Decision Date2007-01-16
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

C-JAWS CERVICAL COMPRESSIVE MINI FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Medicrea Technologies. It received FDA 510(k) clearance on 2007-01-16 under 510(k) number K062181. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C-JAWS CERVICAL COMPRESSIVE MINI FRAME?

C-JAWS CERVICAL COMPRESSIVE MINI FRAME is a medical device that received FDA 510(k) clearance on 2007-01-16. The listed applicant is Medicrea Technologies. The 510(k) number is K062181.

When did C-JAWS CERVICAL COMPRESSIVE MINI FRAME receive FDA 510(k) clearance?

C-JAWS CERVICAL COMPRESSIVE MINI FRAME received FDA 510(k) clearance on 2007-01-16, under 510(k) number K062181.

Who is the listed applicant for C-JAWS CERVICAL COMPRESSIVE MINI FRAME?

The FDA 510(k) record lists Medicrea Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C-JAWS CERVICAL COMPRESSIVE MINI FRAME?

The FDA product code for C-JAWS CERVICAL COMPRESSIVE MINI FRAME is KWP.

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Other records listing Medicrea Technologies as applicant

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Related Devices (Code: KWP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K133094CERTEX OCT SPINAL IMPLANT SYSTEMX-Spine Systems, Inc.K132504TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEMCorelink, LLCK132900MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMIntelligent Implant Systems, LLCK131427LOTUSSpinal Elements, Inc.K132332MOUNTAINEER OCT SPINAL SYSTEMMedos International SARLK131156LANX SPINAL FIXATION SYSTEMLanx, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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