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)

SMALL FRAGMENT PLATES AND SCREWS

K-Number: K951302 · 1995-05-05

ApplicantMedpac
Decision Date1995-05-05
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SMALL FRAGMENT PLATES AND SCREWS is the device name listed in this FDA 510(k) record. The listed applicant is Medpac. It received FDA 510(k) clearance on 1995-05-05 under 510(k) number K951302. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMALL FRAGMENT PLATES AND SCREWS?

SMALL FRAGMENT PLATES AND SCREWS is a medical device that received FDA 510(k) clearance on 1995-05-05. The listed applicant is Medpac. The 510(k) number is K951302.

When did SMALL FRAGMENT PLATES AND SCREWS receive FDA 510(k) clearance?

SMALL FRAGMENT PLATES AND SCREWS received FDA 510(k) clearance on 1995-05-05, under 510(k) number K951302.

Who is the listed applicant for SMALL FRAGMENT PLATES AND SCREWS?

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

What is the FDA product code for SMALL FRAGMENT PLATES AND SCREWS?

The FDA product code for SMALL FRAGMENT PLATES AND SCREWS is JDS.

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 Medpac 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.

K951303SFCK903697HAWAIIAN SUPRACONDYLAR PLATE

Related Devices (Code: JDS)

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.

K243608TRIGEN Stable Lock Nut & WasherSmith & Nephew, Inc.K240061TRIGEN MAX Tibial Nail System; INTERTAN MAX Hip Fracture Nail SystemSmith & Nephew, Inc.K241804TRIGEN INTERTAN 10S Nail SystemSmith & Nephew, Inc.K233150NET BRAND Osteosynthesis Nailing SystemNarang Medical , Ltd.K230761TRIGEN META-NAIL Nail SystemSmith & Nephew, Inc.K201336DePuy Synthes Tibial Nail Advanced, Depuy Synthes Locking Screws Medullary Nails, 4.0 and 5.0mmSynthes (USA) Products, LLC

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.

↑