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FDA 510(k)

PLANMECA PROONE

K-Number: K072244 · 2007-09-21

ApplicantPlanmeca Oy
Decision Date2007-09-21
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLANMECA PROONE is the device name listed in this FDA 510(k) record. The listed applicant is Planmeca Oy. It received FDA 510(k) clearance on 2007-09-21 under 510(k) number K072244. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLANMECA PROONE?

PLANMECA PROONE is a medical device that received FDA 510(k) clearance on 2007-09-21. The listed applicant is Planmeca Oy. The 510(k) number is K072244.

When did PLANMECA PROONE receive FDA 510(k) clearance?

PLANMECA PROONE received FDA 510(k) clearance on 2007-09-21, under 510(k) number K072244.

Who is the listed applicant for PLANMECA PROONE?

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

What is the FDA product code for PLANMECA PROONE?

The FDA product code for PLANMECA PROONE is MUH.

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Other records listing Planmeca Oy as applicant

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.

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Related Devices (Code: MUH)

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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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