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FDA 510(k)

CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER

K-Number: K944946 · 1995-02-01

Decision Date1995-02-01
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Medical Products, Inc.. It received FDA 510(k) clearance on 1995-02-01 under 510(k) number K944946. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER?

CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER is a medical device that received FDA 510(k) clearance on 1995-02-01. The listed applicant is U.S. Medical Products, Inc.. The 510(k) number is K944946.

When did CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER receive FDA 510(k) clearance?

CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER received FDA 510(k) clearance on 1995-02-01, under 510(k) number K944946.

Who is the listed applicant for CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER?

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

What is the FDA product code for CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER?

The FDA product code for CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER is HWE.

Related Clinical Trials

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.

Other records listing U.S. Medical Products, Inc. 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 24 devices →

Related Devices (Code: HWE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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