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FDA 510(k)

ACTAEON PROBE

K-Number: K013429 · 2002-01-11

ApplicantOsteobiologics, Inc.
Decision Date2002-01-11
Product CodeNGR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACTAEON PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Osteobiologics, Inc.. It received FDA 510(k) clearance on 2002-01-11 under 510(k) number K013429. The device is classified under product code NGR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTAEON PROBE?

ACTAEON PROBE is a medical device that received FDA 510(k) clearance on 2002-01-11. The listed applicant is Osteobiologics, Inc.. The 510(k) number is K013429.

When did ACTAEON PROBE receive FDA 510(k) clearance?

ACTAEON PROBE received FDA 510(k) clearance on 2002-01-11, under 510(k) number K013429.

Who is the listed applicant for ACTAEON PROBE?

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

What is the FDA product code for ACTAEON PROBE?

The FDA product code for ACTAEON PROBE is NGR.

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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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