GAP ENDO-EXO MEDULLARY SYSTEM— 510(k) K160545

Substantially Equivalent

Pega Medical, Inc.

FDA 510(k) clearance K160545 for GAP ENDO-EXO MEDULLARY SYSTEM, Substantially Equivalent on 2016-11-23. Applicant: Pega Medical, Inc.. Device class: 2.

Clearance details

Applicant
Pega Medical, Inc.
Product code
Code HSB
Device class
Class 2
Regulation
21 CFR 888.3020
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Laval, CA
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HSB

product code HSB
Death
49
Injury
12,083
Malfunction
6,561
Other
1
Total
18,694

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 →

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