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FDA 510(k)

TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE

K-Number: K926579 · 1993-04-06

ApplicantTechmedica, Inc.
Decision Date1993-04-06
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1993-04-06 under 510(k) number K926579. 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.

Frequently Asked Questions

What is the TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE?

TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE is a medical device that received FDA 510(k) clearance on 1993-04-06. The listed applicant is Techmedica, Inc.. The 510(k) number is K926579.

When did TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE receive FDA 510(k) clearance?

TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE received FDA 510(k) clearance on 1993-04-06, under 510(k) number K926579.

Who is the listed applicant for TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE?

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

What is the FDA product code for TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE?

The FDA product code for TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE is HWC. This falls under the Cardiovascular category.

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Other records listing Techmedica, 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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