SMITH AND NEPHEW REFLECTION 3 ACETABULAR SYSTEM— 510(k) K070756

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K070756 for SMITH AND NEPHEW REFLECTION 3 ACETABULAR SYSTEM, Substantially Equivalent on 2007-06-06. Applicant: Smith & Nephew, Inc.. Device class: 2.

Clearance details

Applicant
Smith & Nephew, Inc.
Product code
Code MBL
Device class
Class 2
Regulation
21 CFR 888.3358
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Memphis, TN, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code MBL

product code MBL
Injury
439
Total
439

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 K070756

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 K070756.

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