Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CARPENTER BONE CLAMP

K-Number: K770118 · 1977-01-26

ApplicantStryker Corp.
Decision Date1977-01-26
Product CodeHXD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARPENTER BONE CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K770118. The device is classified under product code HXD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARPENTER BONE CLAMP?

CARPENTER BONE CLAMP is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Stryker Corp.. The 510(k) number is K770118.

When did CARPENTER BONE CLAMP receive FDA 510(k) clearance?

CARPENTER BONE CLAMP received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770118.

Who is the listed applicant for CARPENTER BONE CLAMP?

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

What is the FDA product code for CARPENTER BONE CLAMP?

The FDA product code for CARPENTER BONE CLAMP is HXD.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stryker Corp. 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.

K230045HipCheckK191259Stryker CrossFlow Integrated Arthroscopy PumpK182359HipCheckK122113MEMORY METAL STAPLES, EASYCLIPK122053SHAPEMATCH CUTTING GUIDEK122284HOFFMANN 3

View all 119 devices →

Related Devices (Code: HXD)

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.

K890368KIDNEY CLAMPKinetic Medical ProductsK890381PARAMETRIUM CLAMPKinetic Medical ProductsK890372INTESTINAL CLAMPKinetic Medical ProductsK890371INTESTINAL CRUSHING CLAMPKinetic Medical ProductsK874959VASCULAR CLAMPSolway, Inc.K872386C CLAMPMed-Tool, Inc.

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.

↑