GRAVITYTM PEEK-OPTIMA Suture Anchor
K-Number: K170265 · 2017-02-23
ApplicantWrightmedicaltechnologyinc
Decision Date2017-02-23
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
GRAVITYTM PEEK-OPTIMA Suture Anchor is a medical device manufactured by Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2017-02-23 under approval number K170265. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the GRAVITYTM PEEK-OPTIMA Suture Anchor?
GRAVITYTM PEEK-OPTIMA Suture Anchor is a medical device that received FDA 510(k) clearance on 2017-02-23. It is manufactured by Wrightmedicaltechnologyinc. The 510(k) number is K170265.
When was GRAVITYTM PEEK-OPTIMA Suture Anchor approved by the FDA?
GRAVITYTM PEEK-OPTIMA Suture Anchor received FDA 510(k) clearance on 2017-02-23, under approval number K170265.
What company makes GRAVITYTM PEEK-OPTIMA Suture Anchor?
GRAVITYTM PEEK-OPTIMA Suture Anchor is manufactured by Wrightmedicaltechnologyinc.
What is the FDA product code for GRAVITYTM PEEK-OPTIMA Suture Anchor?
The FDA product code for GRAVITYTM PEEK-OPTIMA Suture Anchor is MBI.
Related PubMed Literature
Other Devices by Wrightmedicaltechnologyinc
Related Devices (Code: MBI)
K163034SUTUREFIX Curved Suture AnchorSmith and Nephew, Inc.
K162198GFS UltimateParcus Medical, LLC
K162386KATOR Suture AnchorKator, LLC
K161033AFX Femoral Implant With InserterCayenne Medical, Inc.
K160996Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmDunamis, LLC
K161001MILAGRO ADVANCE PEEK Interference ScrewMedos International SARL
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.