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FDA 510(k)

TECHMEDIA BONE STAPLE

K-Number: K813567 · 1982-01-12

ApplicantTechmedica, Inc.
Decision Date1982-01-12
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TECHMEDIA BONE STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1982-01-12 under 510(k) number K813567. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHMEDIA BONE STAPLE?

TECHMEDIA BONE STAPLE is a medical device that received FDA 510(k) clearance on 1982-01-12. The listed applicant is Techmedica, Inc.. The 510(k) number is K813567.

When did TECHMEDIA BONE STAPLE receive FDA 510(k) clearance?

TECHMEDIA BONE STAPLE received FDA 510(k) clearance on 1982-01-12, under 510(k) number K813567.

Who is the listed applicant for TECHMEDIA BONE STAPLE?

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 TECHMEDIA BONE STAPLE?

The FDA product code for TECHMEDIA BONE STAPLE is JDR.

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Other records listing Techmedica, Inc. 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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