Atlas FDA

DEPUY RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT

FDA 510(k) clearance K071016 · decided 2007-09-04

Clearance details

K-number
K071016
Device name
DEPUY RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT
Applicant
DePuy Orthopaedics, Inc.
Decision
Substantially Equivalent
Date received
2007-04-10
Decision date
2007-09-04
Days to decision
147 days
Clearance type
Traditional
Product code
FTM
Device class
2
Regulation number
878.3300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Warsaw, IN, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

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Ceramax Ceramic Hip System (P070026/S123)DePuy Orthopaedics, Inc.2025-12-09
CERAMAX CERAMIC HIP SYSTEM (P070026/S121)DePuy Orthopaedics, Inc.2025-08-05
CERAMAX CERAMIC HIP SYSTEM (P070026/S122)DePuy Orthopaedics, Inc.2025-08-01
CERAMAX® ceramic total hip system (P070026/S120)DePuy Orthopaedics, Inc.2025-06-24
CERAMAX CERAMIC HIP SYSTEM (P070026/S119)DePuy Orthopaedics, Inc.2025-04-04
DePuy Ceramax Ceramic Total Hip System (P070026/S114)DePuy Orthopaedics, Inc.2025-03-19
Ceramax Ceramic Hip System (P070026/S117)DePuy Orthopaedics, Inc.2025-02-21
Ceramax® Ceramic Total Hip System (P070026/S116)DePuy Orthopaedics, Inc.2025-02-11