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FDA 510(k)

NEXMED CANCELLOUS BONE SCREWS

K-Number: K951656 · 1995-07-18

ApplicantNexmed, Inc.
Decision Date1995-07-18
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

NEXMED CANCELLOUS BONE SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Nexmed, Inc.. It received FDA 510(k) clearance on 1995-07-18 under 510(k) number K951656. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the NEXMED CANCELLOUS BONE SCREWS?

NEXMED CANCELLOUS BONE SCREWS is a medical device that received FDA 510(k) clearance on 1995-07-18. The listed applicant is Nexmed, Inc.. The 510(k) number is K951656.

When did NEXMED CANCELLOUS BONE SCREWS receive FDA 510(k) clearance?

NEXMED CANCELLOUS BONE SCREWS received FDA 510(k) clearance on 1995-07-18, under 510(k) number K951656.

Who is the listed applicant for NEXMED CANCELLOUS BONE SCREWS?

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

What is the FDA product code for NEXMED CANCELLOUS BONE SCREWS?

The FDA product code for NEXMED CANCELLOUS BONE SCREWS is HWC. This falls under the Cardiovascular category.

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Other records listing Nexmed, Inc. as applicant

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Related Devices (Code: HWC)

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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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