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FDA 510(k)

BARRIER ORTHOPAEDIC SPLIT SHEET

K-Number: K760896 · 1977-01-05

Decision Date1977-01-05
Product Code
DecisionSubstantially Equivalent

Device Summary

BARRIER ORTHOPAEDIC SPLIT SHEET is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K760896. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER ORTHOPAEDIC SPLIT SHEET?

BARRIER ORTHOPAEDIC SPLIT SHEET is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Surgikos, Inc.. The 510(k) number is K760896.

When did BARRIER ORTHOPAEDIC SPLIT SHEET receive FDA 510(k) clearance?

BARRIER ORTHOPAEDIC SPLIT SHEET received FDA 510(k) clearance on 1977-01-05, under 510(k) number K760896.

Who is the listed applicant for BARRIER ORTHOPAEDIC SPLIT SHEET?

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

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 Surgikos, 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.

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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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