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FDA 510(k)

DEPUY MODIFIED SKELETAL TRACTION PIN

K-Number: K761088 · 1976-12-17

ApplicantDepuy, Inc.
Decision Date1976-12-17
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY MODIFIED SKELETAL TRACTION PIN is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1976-12-17 under 510(k) number K761088. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY MODIFIED SKELETAL TRACTION PIN?

DEPUY MODIFIED SKELETAL TRACTION PIN is a medical device that received FDA 510(k) clearance on 1976-12-17. The listed applicant is Depuy, Inc.. The 510(k) number is K761088.

When did DEPUY MODIFIED SKELETAL TRACTION PIN receive FDA 510(k) clearance?

DEPUY MODIFIED SKELETAL TRACTION PIN received FDA 510(k) clearance on 1976-12-17, under 510(k) number K761088.

Who is the listed applicant for DEPUY MODIFIED SKELETAL TRACTION PIN?

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

What is the FDA product code for DEPUY MODIFIED SKELETAL TRACTION PIN?

The FDA product code for DEPUY MODIFIED SKELETAL TRACTION PIN is JEC.

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 Depuy, 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 303 devices →

Related Devices (Code: JEC)

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

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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