ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE— 510(k) K092201

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K092201 for ADVANCE 913 MEDIAL PIVOT TIBIAL INSERT, ADVANCE 913 MEDIAL PIVOT TIBIAL BASE, Substantially Equivalent on 2009-08-20. Applicant: Wrightmedicaltechnologyinc. Device class: 2.

Clearance details

Applicant
Wrightmedicaltechnologyinc
Product code
Code JWH
Device class
Class 2
Regulation
21 CFR 888.3560
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Arlington, TN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code JWH

product code JWH
Death
26
Injury
51,564
Malfunction
9,725
Other
9
Total
61,324

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K092201

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K092201.

Data sourced from openFDA. This site is unofficial and independent of the FDA.