FDA Device Intelligence
HomeCOLLAGEN MATRIX, INC. › RejuvaKnee

RejuvaKnee

COLLAGEN MATRIX, INC. · Model REJ075 · UDI-DI 00813954026022

OLC Prescription
3
510(k) clearances
7
Adverse events
1
Recalls
6
Facilities

Description

Collagen Meniscus Implant

Recalls

DateFirmReason
2018-01-25Stryker CorporationThe recalled products were shipped without the required temperature control packaging, therefore could potentially have been exposed to elevated temperatures during transit.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.