FDA 510(k), K071092, ASNIS MICRO CANNULATED SCREW

FDA 510(k), K071092, ASNIS MICRO CANNULATED SCREW

Regular price $89.00 USD
Regular price Sale price $89.00 USD
Sale Sold out
510(K) Number: K071092
Device Name: ASNIS MICRO CANNULATED SCREW
Manufacturer:
Device Classification Name: Screw, Fixation, Bone
Regulation Number: 888.3040
Classification Product Code: HWC
Date Received: 04/18/2007
Decision Date: 05/11/2007
Regulation Medical Specialty: Orthopedic

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or additional information requests, internal FDA communications, software and risk analysis, specifications, SOPs, unpublished studies, draft manuals, etc.”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