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FDA 510(k)

CODMAN SKULL PINS (ADULT & CHILD), REUSABLE

K-Number: K912005 · 1991-09-19

Decision Date1991-09-19
Product CodeHBL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN SKULL PINS (ADULT & CHILD), REUSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1991-09-19 under 510(k) number K912005. The device is classified under product code HBL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN SKULL PINS (ADULT & CHILD), REUSABLE?

CODMAN SKULL PINS (ADULT & CHILD), REUSABLE is a medical device that received FDA 510(k) clearance on 1991-09-19. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K912005.

When did CODMAN SKULL PINS (ADULT & CHILD), REUSABLE receive FDA 510(k) clearance?

CODMAN SKULL PINS (ADULT & CHILD), REUSABLE received FDA 510(k) clearance on 1991-09-19, under 510(k) number K912005.

Who is the listed applicant for CODMAN SKULL PINS (ADULT & CHILD), REUSABLE?

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

What is the FDA product code for CODMAN SKULL PINS (ADULT & CHILD), REUSABLE?

The FDA product code for CODMAN SKULL PINS (ADULT & CHILD), REUSABLE is HBL.

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 Codman & Shurtleff, 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 147 devices →

Related Devices (Code: HBL)

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

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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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