Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Reliance Medical Systems, LLC · Predicate Candidate Screening

24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

95 daysmedian FDA review time
296 days90th percentile
24clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K202266Reliance Cervical IBF SystemReliance Medical Systems, LLC2022-03-295950
K210874Reliance Spinal Screw SystemReliance Medical Systems, LLC2021-05-13500
K183049Reliance Lumbar IBF SystemReliance Medical Systems, LLC2019-02-151050
K173283Reliance Lumbar IBF SystemReliance Medical Systems, LLC2018-01-19950
K173102Reliance Cervical IBF SystemReliance Medical Systems, LLC2017-12-29910
K172489Reliance Cervical IBF SystemReliance Medical Systems, LLC2017-09-07210
K162066Reliance Spinal Screw SystemReliance Medical Systems, LLC2016-12-021290
K160463Reliance Lumbar IBF SystemReliance Medical Systems, LLC2016-05-20910
K152131Reliance Spinal Screw SystemReliance Medical Systems, LLC2015-09-17480
K142269Reliance Cervical IBF SystemReliance Medical Systems, LLC2015-06-092980
K142867Reliance Posterior Cervical-Thoracic SystemReliance Medical Systems, LLC2015-04-292100
K142217Reliance Interspinous Plate SystemReliance Medical Systems, LLC2015-04-022330
K140742RELIANCE ANTERIOR CERVICAL PLATEReliance Medical Systems, LLC2014-04-25310
K131429RELIANCE CERVICAL IBF SYSTEMReliance Medical Systems, LLC2013-09-231290
K123521RELIANCE SPINAL SCREW SYSTEMReliance Medical Systems, LLC2013-02-07840
K122292RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEMReliance Medical Systems, LLC2012-10-24850
K122216RELIANCE ANTERIOR CERVICAL PLATE SYSTEMReliance Medical Systems, LLC2012-09-05420
K120396RELIANCE CERVICAL IBF SYSTEMReliance Medical Systems, LLC2012-05-08900
K113540RELIANCE LUMBAR IBF SYSTEMReliance Medical Systems, LLC2012-03-121030
K110896RELIANCE SPINAL SCREW SYSTEMReliance Medical Systems, LLC2012-01-202960
K081978RELIANCE SPINAL SCREW SYSTEMReliance Medical Systems, LLC2009-03-262580
K081383RELIANCE VBS SYSTEMReliance Medical Systems, LLC2008-07-02470
K073349RELIANCE BUTTRESS WASHER SYSTEMReliance Medical Systems, LLC2008-02-13760
K063637RELIANCE VBS SYSTEMReliance Medical Systems, LLC2007-09-272940

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda