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)

METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET

K-Number: K113752 · 2012-02-06

ApplicantSolana Surgical, LLC
Decision Date2012-02-06
Product CodeKWD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Solana Surgical, LLC. It received FDA 510(k) clearance on 2012-02-06 under 510(k) number K113752. The device is classified under product code KWD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET?

METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 2012-02-06. The listed applicant is Solana Surgical, LLC. The 510(k) number is K113752.

When did METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET receive FDA 510(k) clearance?

METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET received FDA 510(k) clearance on 2012-02-06, under 510(k) number K113752.

Who is the listed applicant for METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET?

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

What is the FDA product code for METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET?

The FDA product code for METATARSAL DECOMPRESSION IMPLANT SURGICAL INSTRUMENT SET is KWD.

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 Solana Surgical, LLC 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.

K132594CROSSCHECK PLATING SYSTEMK131187LESSER METATARSAL HEAD IMPLANT SYSTEMK124045FUSEFORCE IMPLANT SYSTEMK122738GAITWAY IMPLANT SYSTEM, SURGICAL INSTRUMENT SETK120390SOLAFIX TWIST SCREW IMPLANT SYSTEM, SURGICAL INSTRUMENT SETK120029HEMI PHALANGEAL IMPLANT SURGICAL INSTRUMENT SET

View all 8 devices →

Related Devices (Code: KWD)

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.

K250074HYALEX® MTP Hemiarthroplasty ImplantHyalex Orthopaedics, Inc.K240268Accu-Joint Hemi ImplantAccufix Surgical, Inc.K221220Montross Extremity Medical Hemi Implant SystemMontross Extremity MedicalK222964BioPoly Lesser Toe Hemiarthroplasty ImplantBioPoly, LLCK201393restor3d MTP ImplantRestor3D, Inc.K203634BioPoly Great Toe Hemiarthroplasty ImplantBioPoly, 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.

↑