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FDA 510(k)

MECTACER BIOLOX FORTE-FEMORAL HEADS

K-Number: K073337 · 2008-02-13

ApplicantMedacta International S.A.
Decision Date2008-02-13
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MECTACER BIOLOX FORTE-FEMORAL HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International S.A.. It received FDA 510(k) clearance on 2008-02-13 under 510(k) number K073337. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MECTACER BIOLOX FORTE-FEMORAL HEADS?

MECTACER BIOLOX FORTE-FEMORAL HEADS is a medical device that received FDA 510(k) clearance on 2008-02-13. The listed applicant is Medacta International S.A.. The 510(k) number is K073337.

When did MECTACER BIOLOX FORTE-FEMORAL HEADS receive FDA 510(k) clearance?

MECTACER BIOLOX FORTE-FEMORAL HEADS received FDA 510(k) clearance on 2008-02-13, under 510(k) number K073337.

Who is the listed applicant for MECTACER BIOLOX FORTE-FEMORAL HEADS?

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

What is the FDA product code for MECTACER BIOLOX FORTE-FEMORAL HEADS?

The FDA product code for MECTACER BIOLOX FORTE-FEMORAL HEADS is LZO.

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Related Devices (Code: LZO)

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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