WATSON-FARRAR TOTAL HIP REPLACEMENT

Prosthesis, Hip, Femoral Component, Cemented, Metal

ORTHOPEDIC EQUIPMENT CO., INC.

The following data is part of a premarket notification filed by Orthopedic Equipment Co., Inc. with the FDA for Watson-farrar Total Hip Replacement.

Pre-market Notification Details

• Device ID: K770219
• 510k Number: K770219
• Device Name: WATSON-FARRAR TOTAL HIP REPLACEMENT
• Classification: Prosthesis, Hip, Femoral Component, Cemented, Metal
• Applicant: ORTHOPEDIC EQUIPMENT CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: JDG
• CFR Regulation Number: 888.3360 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1977-02-03
• Decision Date: 1977-02-17

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00880304256118	K770219	000
00880304255791	K770219	000
00880304255814	K770219	000
00880304255821	K770219	000
00880304255838	K770219	000
00880304255845	K770219	000
00880304255869	K770219	000
00880304255883	K770219	000
00880304255890	K770219	000
00880304255784	K770219	000
00880304255777	K770219	000
00880304011052	K770219	000
00880304011069	K770219	000
00880304011076	K770219	000
00880304255715	K770219	000
00880304255722	K770219	000
00880304255739	K770219	000
00880304255753	K770219	000
00880304255760	K770219	000
00880304255906	K770219	000
00880304255913	K770219	000
00880304256033	K770219	000
00880304256040	K770219	000
00880304256057	K770219	000
00880304256064	K770219	000
00880304256071	K770219	000
00880304256088	K770219	000
00880304256095	K770219	000
00880304256101	K770219	000
00880304256026	K770219	000
00880304256019	K770219	000
00880304255920	K770219	000
00880304255944	K770219	000
00880304255951	K770219	000
00880304255968	K770219	000
00880304255975	K770219	000
00880304255982	K770219	000
00880304255999	K770219	000
00880304256002	K770219	000
00880304001626	K770219	000