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FDA 510(k)

Physica Porous Femoral Components

K-Number: K243615 · 2024-12-18

Decision Date2024-12-18
Product CodeMBH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Physica Porous Femoral Components is the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K243615. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Physica Porous Femoral Components?

Physica Porous Femoral Components is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K243615.

When did Physica Porous Femoral Components receive FDA 510(k) clearance?

Physica Porous Femoral Components received FDA 510(k) clearance on 2024-12-18, under 510(k) number K243615.

Who is the listed applicant for Physica Porous Femoral Components?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Physica Porous Femoral Components?

The FDA product code for Physica Porous Femoral Components is MBH.

Other records listing Lima Corporate S.P.A. 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.

View all 41 devices →

Related Devices (Code: MBH)

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.

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.