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)

SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC

K-Number: K051256 · 2005-07-21

ApplicantNoble Fiber Technologies, Inc.
Decision Date2005-07-21
Product CodeISH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC is the device name listed in this FDA 510(k) record. The listed applicant is Noble Fiber Technologies, Inc.. It received FDA 510(k) clearance on 2005-07-21 under 510(k) number K051256. The device is classified under product code ISH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC?

SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC is a medical device that received FDA 510(k) clearance on 2005-07-21. The listed applicant is Noble Fiber Technologies, Inc.. The 510(k) number is K051256.

When did SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC receive FDA 510(k) clearance?

SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC received FDA 510(k) clearance on 2005-07-21, under 510(k) number K051256.

Who is the listed applicant for SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC?

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

What is the FDA product code for SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC?

The FDA product code for SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC is ISH.

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 Noble Fiber Technologies, 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.

K063190SILVERSEAL WOUND PACKING STRIPS WITH X-STATICK050726SILVERSEAL SILVERAID WITH X-STATICK050649SILVERSEAL CONTACTING WOUND DRESSING WITH X-STATICK043526SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATIC

Related Devices (Code: ISH)

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.

K823396FREE FLEX HEEL HEIGHT ADJUSTOROrthopedic Systems, Inc.K820505ANKLE/FOOT EXTERNALMauch Laboratories, Inc.K791331THE TUCKER-SACH FOOT AND TUCKER-SYME FTKiswood Manufacturing, 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.

↑