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510(k) K122783

PLASMAFIT ACETABULAR CUP AND VITELENE INSERT by Aesculap Implant System, Inc. — Product Code OQG

K122783 is an FDA 510(k) premarket notification submitted by Aesculap Implant System, Inc. for the device "PLASMAFIT ACETABULAR CUP AND VITELENE INSERT". The FDA issued a decision of Substantially Equivalent on October 30, 2013. The device falls under product code OQG (Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented), a Class II device regulated under 21 CFR 888.3358. Aesculap Implant System, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 2013
Date Received
September 11, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
Device Class
Class II
Regulation Number
888.3358
Review Panel
OR
Submission Type

1. Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis. 3. Correction of functional deformity. 4. Treatment of non-union, femoral neck fracture, and trochanteric fractures of the proximal femur with head involvement, unmanageable by other techniques. 5. Revision procedures where other treatment or devices have failed. Cemented and uncemented use.

Other clearances by Aesculap Implant System, Inc.

  • K142707 — AIS Odontoid Fracture Fixation System (December 19, 2014)
  • K142150 — AIS MODULIFT VBR SYSTEM (October 29, 2014)
  • K133802 — AIS MODULIFT VBR SYSTEM (April 17, 2014)
  • K130887 — S4C NAVIGATION INSTRUMENTS (August 13, 2013)
  • K123909 — AESCULAP CESPACE XP (April 15, 2013)
  • K130291 — S4 SPINAL SYSTEM (April 11, 2013)
  • K122985 — COLUMBUS REVISION KNEE SYSTEM (October 26, 2012)
  • K112551 — S4 SPINAL SYSTEM (November 21, 2011)
  • K101281 — VEGA KNEE SYSTEM (July 30, 2010)
  • K100147 — S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM (July 23, 2010)

Other clearances for product code OQG

  • K202705 — Prime and DYNASTY® Additive Manufacturing Shells (August 20, 2021)
  • K203472 — KMTI Hip Replacement System (April 2, 2021)
  • K201660 — KMTI Hip Replacement System, Tesera Trabecular Technologies (T3) Acetabular Shel (July 16, 2020)
  • K200328 — Tesera Trabecular Technologies (T3) Acetabular Shell System, Porous Acetabular C (March 11, 2020)
  • K172651 — FMP Extended Liners (December 13, 2017)
  • K171543 — Renovis Surgical Hip Replacement System (November 16, 2017)
  • K173104 — Klassic HD® Hooded Acetabular Insert with E-Link® Poly, Klassic HD® Low Profile (October 27, 2017)
  • K143647 — Renovis Surgical Hip Replacement System (May 11, 2015)
  • K140130 — X-ALT HIGHLY CROSS LINKED ACETABULAR LINERS WITH VITAMIN E, NEUTRAL, 10 DEGREE H (November 6, 2014)
  • K141972 — KLASSIC HD ACETABULAR INSERT WITH E-LINK POLY (October 9, 2014)

FDA data resources