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FDA 510(k)

AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE

K-Number: K052528 · 2005-10-11

ApplicantCeremed , Inc.
Decision Date2005-10-11
Product CodeMTJ
DecisionSubstantially Equivalent

Device Summary

AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE is the device name listed in this FDA 510(k) record. The listed applicant is Ceremed , Inc.. It received FDA 510(k) clearance on 2005-10-11 under 510(k) number K052528. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE?

AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE is a medical device that received FDA 510(k) clearance on 2005-10-11. The listed applicant is Ceremed , Inc.. The 510(k) number is K052528.

When did AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE receive FDA 510(k) clearance?

AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE received FDA 510(k) clearance on 2005-10-11, under 510(k) number K052528.

Who is the listed applicant for AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE?

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

What is the FDA product code for AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE?

The FDA product code for AOC BONE WAX OSTENE, OSTEOTENE AND CERETENE is MTJ.

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Related Devices (Code: MTJ)

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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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