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FDA 510(k)

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED

K-Number: K925682 · 1994-01-07

ApplicantBiopro, Inc.
Decision Date1994-01-07
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Biopro, Inc.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K925682. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED?

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Biopro, Inc.. The 510(k) number is K925682.

When did BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED receive FDA 510(k) clearance?

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED received FDA 510(k) clearance on 1994-01-07, under 510(k) number K925682.

Who is the listed applicant for BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED?

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

What is the FDA product code for BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED?

The FDA product code for BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED is LZO.

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Other records listing Biopro, Inc. as applicant

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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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