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FDA 510(k)

PTG-05

K-Number: K240347 · 2024-07-21

ApplicantZimmer Medizinsysteme GmbH
Decision Date2024-07-21
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PTG-05 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2024-07-21 under 510(k) number K240347. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTG-05?

PTG-05 is a medical device that received FDA 510(k) clearance on 2024-07-21. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K240347.

When did PTG-05 receive FDA 510(k) clearance?

PTG-05 received FDA 510(k) clearance on 2024-07-21, under 510(k) number K240347.

Who is the listed applicant for PTG-05?

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

What is the FDA product code for PTG-05?

The FDA product code for PTG-05 is NGX.

Other records listing Zimmer Medizinsysteme GmbH as applicant

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Related Devices (Code: NGX)

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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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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