FDA 510(K) K123769, ZX-I POWER ADD ON
FDA 510(K) K123769, ZX-I POWER ADD ON
Device Classification Name Wheelchair, Powered
510(k) Number K123769
Device Name ZX-I POWER ADD ON
Applicant SPINERGY, INC.
Regulation Number 890.3860
Classification Product Code ITI
Date Received 12/07/2012
Decision Date 05/10/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
Total pages: 763
Fully redacted pages: 525
Content pages: 238
Couldn't load pickup availability
PLEASE NOTE: Most 510(k)s obtained through FOIA are heavily redacted, often omitting sections related to testing, software, manufacturing, and other technical data. Please be sure to review the total pages, redacted pages, and content pages listed in the description to get a sense of how much of the document is redacted. As the FDA FOIA office explains: “We HEAVILY REDACT the majority of the following portions of 510(k) filings: testing data, technical data, lab reports, manufacturing information, vendor information, substantive discussions regarding deficiencies or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.” If you’d like more details about a specific document before purchasing, please contact us at info@foiadocs.com.
View full details