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FDA 510(k)

CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON

K-Number: K072327 · 2007-10-24

ApplicantRegeneration Technologies, Inc.
Decision Date2007-10-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON is the device name listed in this FDA 510(k) record. The listed applicant is Regeneration Technologies, Inc.. It received FDA 510(k) clearance on 2007-10-24 under 510(k) number K072327. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON?

CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON is a medical device that received FDA 510(k) clearance on 2007-10-24. The listed applicant is Regeneration Technologies, Inc.. The 510(k) number is K072327.

When did CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON receive FDA 510(k) clearance?

CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON received FDA 510(k) clearance on 2007-10-24, under 510(k) number K072327.

Who is the listed applicant for CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON?

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

What is the FDA product code for CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON?

The FDA product code for CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON is MQV.

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Other records listing Regeneration Technologies, Inc. as applicant

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Related Devices (Code: MQV)

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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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