The following data is part of a premarket notification filed by Orthotic & Prosthetic Lab, Inc. with the FDA for O&p Bivalve Cranial Molding Helmet.
Device ID | K063395 |
510k Number | K063395 |
Device Name: | O&P BIVALVE CRANIAL MOLDING HELMET |
Classification | Orthosis, Cranial |
Applicant | ORTHOTIC & PROSTHETIC LAB, INC. 748 MARSHALL AVE. Webster Groves, MO 63119 |
Contact | Thomas L Malone |
Correspondent | Thomas L Malone ORTHOTIC & PROSTHETIC LAB, INC. 748 MARSHALL AVE. Webster Groves, MO 63119 |
Product Code | MVA |
CFR Regulation Number | 882.5970 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-11-09 |
Decision Date | 2006-12-22 |
Summary: | summary |