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FDA 510(k)

ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION

K-Number: K935295 · 1994-10-11

ApplicantHowmedica Corp.
Decision Date1994-10-11
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1994-10-11 under 510(k) number K935295. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION?

ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-10-11. The listed applicant is Howmedica Corp.. The 510(k) number is K935295.

When did ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION receive FDA 510(k) clearance?

ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION received FDA 510(k) clearance on 1994-10-11, under 510(k) number K935295.

Who is the listed applicant for ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION?

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

What is the FDA product code for ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION?

The FDA product code for ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION is HSB.

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Other records listing Howmedica Corp. as applicant

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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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